Canonical Allele Identifier: CA2114131443

Gene: GGACT PCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.100530272C= , CM000675.2:g.100530272C=	GRCh38
NC_000013.10:g.101182526C= , CM000675.1:g.101182526C=	GRCh37
NC_000013.9:g.99980527C=	NCBI36
NG_008768.1:g.446190C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683975.1:c.*1858G= (GGACT) MANE Select	ENSP00000508020.1:n.*1858G=
ENST00000376285.6:c.*106C= (PCCA) MANE Select	ENSP00000365462.1:n.*106C=
ENST00000636366.1:c.1491C= (PCCA)
ENST00000636475.1:c.1808C= (PCCA)
ENST00000637657.1:c.1953C= (PCCA)
ENST00000647303.1:c.*1777C= (PCCA)	ENSP00000495663.1:n.*1777C=
ENST00000376250.6:c.*1858G= (GGACT)	ENSP00000365426.1:n.*1858G=
ENST00000376279.7:c.*106C= (PCCA)	ENSP00000365456.3:n.*106C=
ENST00000376285.5:c.*106C= (PCCA)	ENSP00000365462.1:n.*106C=
ENST00000376286.8:c.*106C= (PCCA)	ENSP00000365463.4:n.*106C=
ENST00000428969.1:c.442C= (PCCA)	ENSP00000399413.1:n.442C=
ENST00000455100.2:c.*1858G= (GGACT)	ENSP00000410449.1:n.*1858G=
ENST00000458283.5:c.509C= (PCCA)
NM_000282.3:c.*106C= (PCCA)	NP_000273.2:n.*106C=
NM_001127692.2:c.*106C= (PCCA)	NP_001121164.1:n.*106C=
NM_001178004.1:c.*106C= (PCCA)	NP_001171475.1:n.*106C=
NM_001195087.1:c.*1858G= (GGACT)	NP_001182016.1:n.*1858G=
NM_033110.2:c.*1858G= (GGACT)	NP_149101.1:n.*1858G=
XR_931615.1:n.2150C= (PCCA)
NM_001352605.1:c.*106C= (PCCA)	NP_001339534.1:n.*106C=
NM_001352606.1:c.*106C= (PCCA)	NP_001339535.1:n.*106C=
NM_001352607.1:c.*106C= (PCCA)	NP_001339536.1:n.*106C=
NM_001352608.1:c.*106C= (PCCA)	NP_001339537.1:n.*106C=
NM_001352610.1:c.*106C= (PCCA)	NP_001339539.1:n.*106C=
NM_001352611.1:c.*106C= (PCCA)	NP_001339540.1:n.*106C=
NM_001352612.1:c.*106C= (PCCA)	NP_001339541.1:n.*106C=
NR_148027.1:n.2342C= (PCCA)
NR_148028.1:n.2380C= (PCCA)
NR_148029.1:n.2302C= (PCCA)
NR_148030.1:n.2483C= (PCCA)
NR_148031.1:n.2296C= (PCCA)
XM_005254083.2:c.*1858G= (GGACT)	XP_005254140.1:n.*1858G=
XM_011521129.3:c.*1858G= (GGACT)	XP_011519431.1:n.*1858G=
XM_017020609.1:c.*106C= (PCCA)	XP_016876098.1:n.*106C=
XM_017020613.1:c.*221C= (PCCA)	XP_016876102.1:n.*221C=
XR_001749567.1:n.2473C= (PCCA)
XR_001749568.1:n.2560C= (PCCA)
XR_001749569.1:n.2419C= (PCCA)
XR_001749576.1:n.2030C= (PCCA)
XR_001749577.1:n.1927C= (PCCA)
NM_000282.4:c.*106C= (PCCA) MANE Select	NP_000273.2:n.*106C=
NM_001352605.2:c.*106C= (PCCA)	NP_001339534.1:n.*106C=
NM_001352606.2:c.*106C= (PCCA)	NP_001339535.1:n.*106C=
NM_001352607.2:c.*106C= (PCCA)	NP_001339536.1:n.*106C=
NM_001352608.2:c.*106C= (PCCA)	NP_001339537.1:n.*106C=
NM_001352610.2:c.*106C= (PCCA)	NP_001339539.1:n.*106C=
NM_001352611.2:c.*106C= (PCCA)	NP_001339540.1:n.*106C=
NM_001352612.2:c.*106C= (PCCA)	NP_001339541.1:n.*106C=
NR_148027.2:n.2264C= (PCCA)
NR_148028.2:n.2302C= (PCCA)
NR_148029.2:n.2224C= (PCCA)
NR_148030.2:n.2405C= (PCCA)
NR_148031.2:n.2218C= (PCCA)
NM_001127692.3:c.*106C= (PCCA)	NP_001121164.1:n.*106C=
NM_001178004.2:c.*106C= (PCCA)	NP_001171475.1:n.*106C=
NM_001195087.2:c.*1858G= (GGACT) MANE Select	NP_001182016.1:n.*1858G=
NM_033110.3:c.*1858G= (GGACT)	NP_149101.1:n.*1858G=