Canonical Allele Identifier: CA2114131449

Gene: GGACT PCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.100530279G= , CM000675.2:g.100530279G=	GRCh38
NC_000013.10:g.101182533G= , CM000675.1:g.101182533G=	GRCh37
NC_000013.9:g.99980534G=	NCBI36
NG_008768.1:g.446197G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683975.1:c.*1851C= (GGACT) MANE Select	ENSP00000508020.1:n.*1851C=
ENST00000376285.6:c.*113G= (PCCA) MANE Select	ENSP00000365462.1:n.*113G=
ENST00000636366.1:c.1498G= (PCCA)
ENST00000636475.1:c.1815G= (PCCA)
ENST00000637657.1:c.1960G= (PCCA)
ENST00000647303.1:c.*1784G= (PCCA)	ENSP00000495663.1:n.*1784G=
ENST00000376250.6:c.*1851C= (GGACT)	ENSP00000365426.1:n.*1851C=
ENST00000376279.7:c.*113G= (PCCA)	ENSP00000365456.3:n.*113G=
ENST00000376285.5:c.*113G= (PCCA)	ENSP00000365462.1:n.*113G=
ENST00000376286.8:c.*113G= (PCCA)	ENSP00000365463.4:n.*113G=
ENST00000428969.1:c.449G= (PCCA)	ENSP00000399413.1:n.449G=
ENST00000455100.2:c.*1851C= (GGACT)	ENSP00000410449.1:n.*1851C=
ENST00000458283.5:c.516G= (PCCA)
NM_000282.3:c.*113G= (PCCA)	NP_000273.2:n.*113G=
NM_001127692.2:c.*113G= (PCCA)	NP_001121164.1:n.*113G=
NM_001178004.1:c.*113G= (PCCA)	NP_001171475.1:n.*113G=
NM_001195087.1:c.*1851C= (GGACT)	NP_001182016.1:n.*1851C=
NM_033110.2:c.*1851C= (GGACT)	NP_149101.1:n.*1851C=
XR_931615.1:n.2157G= (PCCA)
NM_001352605.1:c.*113G= (PCCA)	NP_001339534.1:n.*113G=
NM_001352606.1:c.*113G= (PCCA)	NP_001339535.1:n.*113G=
NM_001352607.1:c.*113G= (PCCA)	NP_001339536.1:n.*113G=
NM_001352608.1:c.*113G= (PCCA)	NP_001339537.1:n.*113G=
NM_001352610.1:c.*113G= (PCCA)	NP_001339539.1:n.*113G=
NM_001352611.1:c.*113G= (PCCA)	NP_001339540.1:n.*113G=
NM_001352612.1:c.*113G= (PCCA)	NP_001339541.1:n.*113G=
NR_148027.1:n.2349G= (PCCA)
NR_148028.1:n.2387G= (PCCA)
NR_148029.1:n.2309G= (PCCA)
NR_148030.1:n.2490G= (PCCA)
NR_148031.1:n.2303G= (PCCA)
XM_005254083.2:c.*1851C= (GGACT)	XP_005254140.1:n.*1851C=
XM_011521129.3:c.*1851C= (GGACT)	XP_011519431.1:n.*1851C=
XM_017020609.1:c.*113G= (PCCA)	XP_016876098.1:n.*113G=
XM_017020613.1:c.*228G= (PCCA)	XP_016876102.1:n.*228G=
XR_001749567.1:n.2480G= (PCCA)
XR_001749568.1:n.2567G= (PCCA)
XR_001749569.1:n.2426G= (PCCA)
XR_001749576.1:n.2037G= (PCCA)
XR_001749577.1:n.1934G= (PCCA)
NM_000282.4:c.*113G= (PCCA) MANE Select	NP_000273.2:n.*113G=
NM_001352605.2:c.*113G= (PCCA)	NP_001339534.1:n.*113G=
NM_001352606.2:c.*113G= (PCCA)	NP_001339535.1:n.*113G=
NM_001352607.2:c.*113G= (PCCA)	NP_001339536.1:n.*113G=
NM_001352608.2:c.*113G= (PCCA)	NP_001339537.1:n.*113G=
NM_001352610.2:c.*113G= (PCCA)	NP_001339539.1:n.*113G=
NM_001352611.2:c.*113G= (PCCA)	NP_001339540.1:n.*113G=
NM_001352612.2:c.*113G= (PCCA)	NP_001339541.1:n.*113G=
NR_148027.2:n.2271G= (PCCA)
NR_148028.2:n.2309G= (PCCA)
NR_148029.2:n.2231G= (PCCA)
NR_148030.2:n.2412G= (PCCA)
NR_148031.2:n.2225G= (PCCA)
NM_001127692.3:c.*113G= (PCCA)	NP_001121164.1:n.*113G=
NM_001178004.2:c.*113G= (PCCA)	NP_001171475.1:n.*113G=
NM_001195087.2:c.*1851C= (GGACT) MANE Select	NP_001182016.1:n.*1851C=
NM_033110.3:c.*1851C= (GGACT)	NP_149101.1:n.*1851C=