Canonical Allele Identifier: CA1286884517

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428540A= , CM000664.2:g.127428540A=	GRCh38
NC_000002.11:g.128186116A= , CM000664.1:g.128186116A=	GRCh37
NC_000002.10:g.127902586A=	NCBI36
NG_016323.1:g.15121A= , LRG_599:g.15121A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.980A= MANE Select	ENSP00000234071.4:p.Glu327=
ENST00000234071.7:c.980A=	ENSP00000234071.3:p.Glu327=
ENST00000402125.2:c.304A=
ENST00000409048.1:c.1082A=	ENSP00000386679.1:p.Glu361=
NM_000312.3:c.980A= , LRG_599t1:c.980A=	NP_000303.1:p.Glu327=
XM_005263715.3:c.1163A=	XP_005263772.1:p.Glu388=
XM_005263716.3:c.1145A=	XP_005263773.1:p.Glu382=
XM_005263717.3:c.1043A=	XP_005263774.1:p.Glu348=
XR_923313.1:n.1332-276T=
XM_005263717.4:c.1043A=	XP_005263774.1:p.Glu348=
XM_017004505.1:c.1223A=	XP_016859994.1:p.Glu408=
XM_024453002.1:c.1325A=	XP_024308770.1:p.Glu442=
XM_024453003.1:c.1265A=	XP_024308771.1:p.Glu422=
XM_024453004.1:c.1163A=	XP_024308772.1:p.Glu388=
XM_024453005.1:c.1145A=	XP_024308773.1:p.Glu382=
XM_024453006.1:c.1082A=	XP_024308774.1:p.Glu361=
XR_001739705.1:n.3607-276T=
XR_923313.2:n.4043-276T=
NM_000312.4:c.980A= MANE Select	NP_000303.1:p.Glu327=
NM_001375602.1:c.1163A=	NP_001362531.1:p.Glu388=
NM_001375603.1:c.1145A=	NP_001362532.1:p.Glu382=
NM_001375604.1:c.1043A=	NP_001362533.1:p.Glu348=
NM_001375605.1:c.1082A=	NP_001362534.1:p.Glu361=
NM_001375606.1:c.1148A=	NP_001362535.1:p.Glu383=
NM_001375607.1:c.1166A=	NP_001362536.1:p.Glu389=
NM_001375608.1:c.923A=	NP_001362537.1:p.Glu308=
NM_001375609.1:c.956A=	NP_001362538.1:p.Glu319=
NM_001375610.1:c.974A=	NP_001362539.1:p.Glu325=
NM_001375611.1:c.980A=	NP_001362540.1:p.Glu327=
NM_001375613.1:c.980A=	NP_001362542.1:p.Glu327=