Canonical Allele Identifier: CA2114131400

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.100530194_100530199delinsCAATTT , CM000675.2:g.100530194_100530199delinsCAATTT GRCh38
NC_000013.10:g.101182448_101182453delinsCAATTT , CM000675.1:g.101182448_101182453delinsCAATTT GRCh37
NC_000013.9:g.99980449_99980454delinsCAATTT NCBI36
NG_008768.1:g.446112_446117delinsCAATTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000683975.1:c.*1931_*1936delinsAAATTG (GGACT) MANE Select ENSP00000508020.1:n.*1931_*1936delinsAAATTG
ENST00000376285.6:c.*28_*33delinsCAATTT (PCCA) MANE Select ENSP00000365462.1:n.*28_*33delinsCAATTT
ENST00000636366.1:c.1413_1418delinsCAATTT (PCCA)
ENST00000636475.1:c.1730_1735delinsCAATTT (PCCA)
ENST00000637657.1:c.1875_1880delinsCAATTT (PCCA)
ENST00000647303.1:c.*1699_*1704delinsCAATTT (PCCA) ENSP00000495663.1:n.*1699_*1704delinsCAATTT
ENST00000376250.6:c.*1931_*1936delinsAAATTG (GGACT) ENSP00000365426.1:n.*1931_*1936delinsAAATTG
ENST00000376279.7:c.*28_*33delinsCAATTT (PCCA) ENSP00000365456.3:n.*28_*33delinsCAATTT
ENST00000376285.5:c.*28_*33delinsCAATTT (PCCA) ENSP00000365462.1:n.*28_*33delinsCAATTT
ENST00000376286.8:c.*28_*33delinsCAATTT (PCCA) ENSP00000365463.4:n.*28_*33delinsCAATTT
ENST00000428969.1:c.364_369delinsCAATTT (PCCA) ENSP00000399413.1:n.364_369delinsCAATTT
ENST00000455100.2:c.*1931_*1936delinsAAATTG (GGACT) ENSP00000410449.1:n.*1931_*1936delinsAAATTG
ENST00000458283.5:c.431_436delinsCAATTT (PCCA)
NM_000282.3:c.*28_*33delinsCAATTT (PCCA) NP_000273.2:n.*28_*33delinsCAATTT
NM_001127692.2:c.*28_*33delinsCAATTT (PCCA) NP_001121164.1:n.*28_*33delinsCAATTT
NM_001178004.1:c.*28_*33delinsCAATTT (PCCA) NP_001171475.1:n.*28_*33delinsCAATTT
NM_001195087.1:c.*1931_*1936delinsAAATTG (GGACT) NP_001182016.1:n.*1931_*1936delinsAAATTG
NM_033110.2:c.*1931_*1936delinsAAATTG (GGACT) NP_149101.1:n.*1931_*1936delinsAAATTG
XR_931615.1:n.2072_2077delinsCAATTT (PCCA)
NM_001352605.1:c.*28_*33delinsCAATTT (PCCA) NP_001339534.1:n.*28_*33delinsCAATTT
NM_001352606.1:c.*28_*33delinsCAATTT (PCCA) NP_001339535.1:n.*28_*33delinsCAATTT
NM_001352607.1:c.*28_*33delinsCAATTT (PCCA) NP_001339536.1:n.*28_*33delinsCAATTT
NM_001352608.1:c.*28_*33delinsCAATTT (PCCA) NP_001339537.1:n.*28_*33delinsCAATTT
NM_001352610.1:c.*28_*33delinsCAATTT (PCCA) NP_001339539.1:n.*28_*33delinsCAATTT
NM_001352611.1:c.*28_*33delinsCAATTT (PCCA) NP_001339540.1:n.*28_*33delinsCAATTT
NM_001352612.1:c.*28_*33delinsCAATTT (PCCA) NP_001339541.1:n.*28_*33delinsCAATTT
NR_148027.1:n.2264_2269delinsCAATTT (PCCA)
NR_148028.1:n.2302_2307delinsCAATTT (PCCA)
NR_148029.1:n.2224_2229delinsCAATTT (PCCA)
NR_148030.1:n.2405_2410delinsCAATTT (PCCA)
NR_148031.1:n.2218_2223delinsCAATTT (PCCA)
XM_005254083.2:c.*1931_*1936delinsAAATTG (GGACT) XP_005254140.1:n.*1931_*1936delinsAAATTG
XM_011521129.3:c.*1931_*1936delinsAAATTG (GGACT) XP_011519431.1:n.*1931_*1936delinsAAATTG
XM_017020609.1:c.*28_*33delinsCAATTT (PCCA) XP_016876098.1:n.*28_*33delinsCAATTT
XM_017020613.1:c.*143_*148delinsCAATTT (PCCA) XP_016876102.1:n.*143_*148delinsCAATTT
XR_001749567.1:n.2395_2400delinsCAATTT (PCCA)
XR_001749568.1:n.2482_2487delinsCAATTT (PCCA)
XR_001749569.1:n.2341_2346delinsCAATTT (PCCA)
XR_001749576.1:n.1952_1957delinsCAATTT (PCCA)
XR_001749577.1:n.1849_1854delinsCAATTT (PCCA)
NM_000282.4:c.*28_*33delinsCAATTT (PCCA) MANE Select NP_000273.2:n.*28_*33delinsCAATTT
NM_001352605.2:c.*28_*33delinsCAATTT (PCCA) NP_001339534.1:n.*28_*33delinsCAATTT
NM_001352606.2:c.*28_*33delinsCAATTT (PCCA) NP_001339535.1:n.*28_*33delinsCAATTT
NM_001352607.2:c.*28_*33delinsCAATTT (PCCA) NP_001339536.1:n.*28_*33delinsCAATTT
NM_001352608.2:c.*28_*33delinsCAATTT (PCCA) NP_001339537.1:n.*28_*33delinsCAATTT
NM_001352610.2:c.*28_*33delinsCAATTT (PCCA) NP_001339539.1:n.*28_*33delinsCAATTT
NM_001352611.2:c.*28_*33delinsCAATTT (PCCA) NP_001339540.1:n.*28_*33delinsCAATTT
NM_001352612.2:c.*28_*33delinsCAATTT (PCCA) NP_001339541.1:n.*28_*33delinsCAATTT
NR_148027.2:n.2186_2191delinsCAATTT (PCCA)
NR_148028.2:n.2224_2229delinsCAATTT (PCCA)
NR_148029.2:n.2146_2151delinsCAATTT (PCCA)
NR_148030.2:n.2327_2332delinsCAATTT (PCCA)
NR_148031.2:n.2140_2145delinsCAATTT (PCCA)
NM_001127692.3:c.*28_*33delinsCAATTT (PCCA) NP_001121164.1:n.*28_*33delinsCAATTT
NM_001178004.2:c.*28_*33delinsCAATTT (PCCA) NP_001171475.1:n.*28_*33delinsCAATTT
NM_001195087.2:c.*1931_*1936delinsAAATTG (GGACT) MANE Select NP_001182016.1:n.*1931_*1936delinsAAATTG
NM_033110.3:c.*1931_*1936delinsAAATTG (GGACT) NP_149101.1:n.*1931_*1936delinsAAATTG