Canonical Allele Identifier: CA2114131337

Gene: PCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.100530077_100530078delinsCT , CM000675.2:g.100530077_100530078delinsCT	GRCh38
NC_000013.10:g.101182331_101182332delinsCT , CM000675.1:g.101182331_101182332delinsCT	GRCh37
NC_000013.9:g.99980332_99980333delinsCT	NCBI36
NG_008768.1:g.445995_445996delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376285.6:c.2119-21_2119-20delinsCT MANE Select	ENSP00000365462.1:n.2119-21_2119-20delinsCT
ENST00000636366.1:c.1317-21_1317-20delinsCT
ENST00000636475.1:c.1634-21_1634-20delinsCT
ENST00000637657.1:c.1779-21_1779-20delinsCT
ENST00000647303.1:c.*1603-21_*1603-20delinsCT	ENSP00000495663.1:n.*1603-21_*1603-20delinsCT
ENST00000376279.7:c.1978-21_1978-20delinsCT	ENSP00000365456.3:n.1978-21_1978-20delinsCT
ENST00000376285.5:c.2119-21_2119-20delinsCT	ENSP00000365462.1:n.2119-21_2119-20delinsCT
ENST00000376286.8:c.2041-21_2041-20delinsCT	ENSP00000365463.4:n.2041-21_2041-20delinsCT
ENST00000428969.1:c.268-21_268-20delinsCT	ENSP00000399413.1:n.268-21_268-20delinsCT
ENST00000458283.5:c.335-21_335-20delinsCT
NM_000282.3:c.2119-21_2119-20delinsCT	NP_000273.2:n.2119-21_2119-20delinsCT
NM_001127692.2:c.2041-21_2041-20delinsCT	NP_001121164.1:n.2041-21_2041-20delinsCT
NM_001178004.1:c.1978-21_1978-20delinsCT	NP_001171475.1:n.1978-21_1978-20delinsCT
XR_931615.1:n.1976-21_1976-20delinsCT
NM_001352605.1:c.2065-21_2065-20delinsCT	NP_001339534.1:n.2065-21_2065-20delinsCT
NM_001352606.1:c.1975-21_1975-20delinsCT	NP_001339535.1:n.1975-21_1975-20delinsCT
NM_001352607.1:c.1900-21_1900-20delinsCT	NP_001339536.1:n.1900-21_1900-20delinsCT
NM_001352608.1:c.1897-21_1897-20delinsCT	NP_001339537.1:n.1897-21_1897-20delinsCT
NM_001352610.1:c.1174-21_1174-20delinsCT	NP_001339539.1:n.1174-21_1174-20delinsCT
NM_001352611.1:c.1120-21_1120-20delinsCT	NP_001339540.1:n.1120-21_1120-20delinsCT
NM_001352612.1:c.1030-21_1030-20delinsCT	NP_001339541.1:n.1030-21_1030-20delinsCT
NR_148027.1:n.2168-21_2168-20delinsCT
NR_148028.1:n.2206-21_2206-20delinsCT
NR_148029.1:n.2128-21_2128-20delinsCT
NR_148030.1:n.2309-21_2309-20delinsCT
NR_148031.1:n.2122-21_2122-20delinsCT
XM_017020609.1:c.2020-21_2020-20delinsCT	XP_016876098.1:n.2020-21_2020-20delinsCT
XM_017020613.1:c.*47-21_*47-20delinsCT	XP_016876102.1:n.*47-21_*47-20delinsCT
XR_001749567.1:n.2299-21_2299-20delinsCT
XR_001749568.1:n.2386-21_2386-20delinsCT
XR_001749569.1:n.2245-21_2245-20delinsCT
XR_001749576.1:n.1856-21_1856-20delinsCT
XR_001749577.1:n.1753-21_1753-20delinsCT
NM_000282.4:c.2119-21_2119-20delinsCT MANE Select	NP_000273.2:n.2119-21_2119-20delinsCT
NM_001352605.2:c.2065-21_2065-20delinsCT	NP_001339534.1:n.2065-21_2065-20delinsCT
NM_001352606.2:c.1975-21_1975-20delinsCT	NP_001339535.1:n.1975-21_1975-20delinsCT
NM_001352607.2:c.1900-21_1900-20delinsCT	NP_001339536.1:n.1900-21_1900-20delinsCT
NM_001352608.2:c.1897-21_1897-20delinsCT	NP_001339537.1:n.1897-21_1897-20delinsCT
NM_001352610.2:c.1174-21_1174-20delinsCT	NP_001339539.1:n.1174-21_1174-20delinsCT
NM_001352611.2:c.1120-21_1120-20delinsCT	NP_001339540.1:n.1120-21_1120-20delinsCT
NM_001352612.2:c.1030-21_1030-20delinsCT	NP_001339541.1:n.1030-21_1030-20delinsCT
NR_148027.2:n.2090-21_2090-20delinsCT
NR_148028.2:n.2128-21_2128-20delinsCT
NR_148029.2:n.2050-21_2050-20delinsCT
NR_148030.2:n.2231-21_2231-20delinsCT
NR_148031.2:n.2044-21_2044-20delinsCT
NM_001127692.3:c.2041-21_2041-20delinsCT	NP_001121164.1:n.2041-21_2041-20delinsCT
NM_001178004.2:c.1978-21_1978-20delinsCT	NP_001171475.1:n.1978-21_1978-20delinsCT