Canonical Allele Identifier: CA2623563083

Gene: GGACT PCCA

Linked Data

• gnomAD v4: 13-100530255-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.100530255A>G , CM000675.2:g.100530255A>G	GRCh38
NC_000013.10:g.101182509A>G , CM000675.1:g.101182509A>G	GRCh37
NC_000013.9:g.99980510A>G	NCBI36
NG_008768.1:g.446173A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683975.1:c.*1875T>C (GGACT) MANE Select	ENSP00000508020.1:n.*1875T>C
ENST00000376285.6:c.*89A>G (PCCA) MANE Select	ENSP00000365462.1:n.*89A>G
ENST00000636366.1:c.1474A>G (PCCA)
ENST00000636475.1:c.1791A>G (PCCA)
ENST00000637657.1:c.1936A>G (PCCA)
ENST00000647303.1:c.*1760A>G (PCCA)	ENSP00000495663.1:n.*1760A>G
ENST00000376250.6:c.*1875T>C (GGACT)	ENSP00000365426.1:n.*1875T>C
ENST00000376279.7:c.*89A>G (PCCA)	ENSP00000365456.3:n.*89A>G
ENST00000376285.5:c.*89A>G (PCCA)	ENSP00000365462.1:n.*89A>G
ENST00000376286.8:c.*89A>G (PCCA)	ENSP00000365463.4:n.*89A>G
ENST00000428969.1:c.425A>G (PCCA)	ENSP00000399413.1:n.425A>G
ENST00000455100.2:c.*1875T>C (GGACT)	ENSP00000410449.1:n.*1875T>C
ENST00000458283.5:c.492A>G (PCCA)
NM_000282.3:c.*89A>G (PCCA)	NP_000273.2:n.*89A>G
NM_001127692.2:c.*89A>G (PCCA)	NP_001121164.1:n.*89A>G
NM_001178004.1:c.*89A>G (PCCA)	NP_001171475.1:n.*89A>G
NM_001195087.1:c.*1875T>C (GGACT)	NP_001182016.1:n.*1875T>C
NM_033110.2:c.*1875T>C (GGACT)	NP_149101.1:n.*1875T>C
XR_931615.1:n.2133A>G (PCCA)
NM_001352605.1:c.*89A>G (PCCA)	NP_001339534.1:n.*89A>G
NM_001352606.1:c.*89A>G (PCCA)	NP_001339535.1:n.*89A>G
NM_001352607.1:c.*89A>G (PCCA)	NP_001339536.1:n.*89A>G
NM_001352608.1:c.*89A>G (PCCA)	NP_001339537.1:n.*89A>G
NM_001352610.1:c.*89A>G (PCCA)	NP_001339539.1:n.*89A>G
NM_001352611.1:c.*89A>G (PCCA)	NP_001339540.1:n.*89A>G
NM_001352612.1:c.*89A>G (PCCA)	NP_001339541.1:n.*89A>G
NR_148027.1:n.2325A>G (PCCA)
NR_148028.1:n.2363A>G (PCCA)
NR_148029.1:n.2285A>G (PCCA)
NR_148030.1:n.2466A>G (PCCA)
NR_148031.1:n.2279A>G (PCCA)
XM_005254083.2:c.*1875T>C (GGACT)	XP_005254140.1:n.*1875T>C
XM_011521129.3:c.*1875T>C (GGACT)	XP_011519431.1:n.*1875T>C
XM_017020609.1:c.*89A>G (PCCA)	XP_016876098.1:n.*89A>G
XM_017020613.1:c.*204A>G (PCCA)	XP_016876102.1:n.*204A>G
XR_001749567.1:n.2456A>G (PCCA)
XR_001749568.1:n.2543A>G (PCCA)
XR_001749569.1:n.2402A>G (PCCA)
XR_001749576.1:n.2013A>G (PCCA)
XR_001749577.1:n.1910A>G (PCCA)
NM_000282.4:c.*89A>G (PCCA) MANE Select	NP_000273.2:n.*89A>G
NM_001352605.2:c.*89A>G (PCCA)	NP_001339534.1:n.*89A>G
NM_001352606.2:c.*89A>G (PCCA)	NP_001339535.1:n.*89A>G
NM_001352607.2:c.*89A>G (PCCA)	NP_001339536.1:n.*89A>G
NM_001352608.2:c.*89A>G (PCCA)	NP_001339537.1:n.*89A>G
NM_001352610.2:c.*89A>G (PCCA)	NP_001339539.1:n.*89A>G
NM_001352611.2:c.*89A>G (PCCA)	NP_001339540.1:n.*89A>G
NM_001352612.2:c.*89A>G (PCCA)	NP_001339541.1:n.*89A>G
NR_148027.2:n.2247A>G (PCCA)
NR_148028.2:n.2285A>G (PCCA)
NR_148029.2:n.2207A>G (PCCA)
NR_148030.2:n.2388A>G (PCCA)
NR_148031.2:n.2201A>G (PCCA)
NM_001127692.3:c.*89A>G (PCCA)	NP_001121164.1:n.*89A>G
NM_001178004.2:c.*89A>G (PCCA)	NP_001171475.1:n.*89A>G
NM_001195087.2:c.*1875T>C (GGACT) MANE Select	NP_001182016.1:n.*1875T>C
NM_033110.3:c.*1875T>C (GGACT)	NP_149101.1:n.*1875T>C