Canonical Allele Identifier: CA255373078

Gene: GGACT PCCA

Linked Data

• dbSNP Id: rs1016530509
• gnomAD v4: 13-100530207-C-A
• MyVariant Identifiers: chr13:g.101182461C>A (hg19) ; chr13:g.100530207C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.100530207C>A , CM000675.2:g.100530207C>A	GRCh38
NC_000013.10:g.101182461C>A , CM000675.1:g.101182461C>A	GRCh37
NC_000013.9:g.99980462C>A	NCBI36
NG_008768.1:g.446125C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683975.1:c.*1923G>T (GGACT) MANE Select	ENSP00000508020.1:n.*1923G>T
ENST00000376285.6:c.*41C>A (PCCA) MANE Select	ENSP00000365462.1:n.*41C>A
ENST00000636366.1:c.1426C>A (PCCA)
ENST00000636475.1:c.1743C>A (PCCA)
ENST00000637657.1:c.1888C>A (PCCA)
ENST00000647303.1:c.*1712C>A (PCCA)	ENSP00000495663.1:n.*1712C>A
ENST00000376250.6:c.*1923G>T (GGACT)	ENSP00000365426.1:n.*1923G>T
ENST00000376279.7:c.*41C>A (PCCA)	ENSP00000365456.3:n.*41C>A
ENST00000376285.5:c.*41C>A (PCCA)	ENSP00000365462.1:n.*41C>A
ENST00000376286.8:c.*41C>A (PCCA)	ENSP00000365463.4:n.*41C>A
ENST00000428969.1:c.377C>A (PCCA)	ENSP00000399413.1:n.377C>A
ENST00000455100.2:c.*1923G>T (GGACT)	ENSP00000410449.1:n.*1923G>T
ENST00000458283.5:c.444C>A (PCCA)
NM_000282.3:c.*41C>A (PCCA)	NP_000273.2:n.*41C>A
NM_001127692.2:c.*41C>A (PCCA)	NP_001121164.1:n.*41C>A
NM_001178004.1:c.*41C>A (PCCA)	NP_001171475.1:n.*41C>A
NM_001195087.1:c.*1923G>T (GGACT)	NP_001182016.1:n.*1923G>T
NM_033110.2:c.*1923G>T (GGACT)	NP_149101.1:n.*1923G>T
XR_931615.1:n.2085C>A (PCCA)
NM_001352605.1:c.*41C>A (PCCA)	NP_001339534.1:n.*41C>A
NM_001352606.1:c.*41C>A (PCCA)	NP_001339535.1:n.*41C>A
NM_001352607.1:c.*41C>A (PCCA)	NP_001339536.1:n.*41C>A
NM_001352608.1:c.*41C>A (PCCA)	NP_001339537.1:n.*41C>A
NM_001352610.1:c.*41C>A (PCCA)	NP_001339539.1:n.*41C>A
NM_001352611.1:c.*41C>A (PCCA)	NP_001339540.1:n.*41C>A
NM_001352612.1:c.*41C>A (PCCA)	NP_001339541.1:n.*41C>A
NR_148027.1:n.2277C>A (PCCA)
NR_148028.1:n.2315C>A (PCCA)
NR_148029.1:n.2237C>A (PCCA)
NR_148030.1:n.2418C>A (PCCA)
NR_148031.1:n.2231C>A (PCCA)
XM_005254083.2:c.*1923G>T (GGACT)	XP_005254140.1:n.*1923G>T
XM_011521129.3:c.*1923G>T (GGACT)	XP_011519431.1:n.*1923G>T
XM_017020609.1:c.*41C>A (PCCA)	XP_016876098.1:n.*41C>A
XM_017020613.1:c.*156C>A (PCCA)	XP_016876102.1:n.*156C>A
XR_001749567.1:n.2408C>A (PCCA)
XR_001749568.1:n.2495C>A (PCCA)
XR_001749569.1:n.2354C>A (PCCA)
XR_001749576.1:n.1965C>A (PCCA)
XR_001749577.1:n.1862C>A (PCCA)
NM_000282.4:c.*41C>A (PCCA) MANE Select	NP_000273.2:n.*41C>A
NM_001352605.2:c.*41C>A (PCCA)	NP_001339534.1:n.*41C>A
NM_001352606.2:c.*41C>A (PCCA)	NP_001339535.1:n.*41C>A
NM_001352607.2:c.*41C>A (PCCA)	NP_001339536.1:n.*41C>A
NM_001352608.2:c.*41C>A (PCCA)	NP_001339537.1:n.*41C>A
NM_001352610.2:c.*41C>A (PCCA)	NP_001339539.1:n.*41C>A
NM_001352611.2:c.*41C>A (PCCA)	NP_001339540.1:n.*41C>A
NM_001352612.2:c.*41C>A (PCCA)	NP_001339541.1:n.*41C>A
NR_148027.2:n.2199C>A (PCCA)
NR_148028.2:n.2237C>A (PCCA)
NR_148029.2:n.2159C>A (PCCA)
NR_148030.2:n.2340C>A (PCCA)
NR_148031.2:n.2153C>A (PCCA)
NM_001127692.3:c.*41C>A (PCCA)	NP_001121164.1:n.*41C>A
NM_001178004.2:c.*41C>A (PCCA)	NP_001171475.1:n.*41C>A
NM_001195087.2:c.*1923G>T (GGACT) MANE Select	NP_001182016.1:n.*1923G>T
NM_033110.3:c.*1923G>T (GGACT)	NP_149101.1:n.*1923G>T