Canonical Allele Identifier: CA1286884480

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428449G= , CM000664.2:g.127428449G=	GRCh38
NC_000002.11:g.128186025G= , CM000664.1:g.128186025G=	GRCh37
NC_000002.10:g.127902495G=	NCBI36
NG_016323.1:g.15030G= , LRG_599:g.15030G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.889G= MANE Select	ENSP00000234071.4:p.Asp297=
ENST00000234071.7:c.889G=	ENSP00000234071.3:p.Asp297=
ENST00000402125.2:c.213G=
ENST00000409048.1:c.991G=	ENSP00000386679.1:p.Asp331=
NM_000312.3:c.889G= , LRG_599t1:c.889G=	NP_000303.1:p.Asp297=
XM_005263715.3:c.1072G=	XP_005263772.1:p.Asp358=
XM_005263716.3:c.1054G=	XP_005263773.1:p.Asp352=
XM_005263717.3:c.952G=	XP_005263774.1:p.Asp318=
XR_923313.1:n.1332-185C=
XM_005263717.4:c.952G=	XP_005263774.1:p.Asp318=
XM_017004505.1:c.1132G=	XP_016859994.1:p.Asp378=
XM_024453002.1:c.1234G=	XP_024308770.1:p.Asp412=
XM_024453003.1:c.1174G=	XP_024308771.1:p.Asp392=
XM_024453004.1:c.1072G=	XP_024308772.1:p.Asp358=
XM_024453005.1:c.1054G=	XP_024308773.1:p.Asp352=
XM_024453006.1:c.991G=	XP_024308774.1:p.Asp331=
XR_001739705.1:n.3607-185C=
XR_923313.2:n.4043-185C=
NM_000312.4:c.889G= MANE Select	NP_000303.1:p.Asp297=
NM_001375602.1:c.1072G=	NP_001362531.1:p.Asp358=
NM_001375603.1:c.1054G=	NP_001362532.1:p.Asp352=
NM_001375604.1:c.952G=	NP_001362533.1:p.Asp318=
NM_001375605.1:c.991G=	NP_001362534.1:p.Asp331=
NM_001375606.1:c.1057G=	NP_001362535.1:p.Asp353=
NM_001375607.1:c.1075G=	NP_001362536.1:p.Asp359=
NM_001375608.1:c.832G=	NP_001362537.1:p.Asp278=
NM_001375609.1:c.865G=	NP_001362538.1:p.Asp289=
NM_001375610.1:c.883G=	NP_001362539.1:p.Asp295=
NM_001375611.1:c.889G=	NP_001362540.1:p.Asp297=
NM_001375613.1:c.889G=	NP_001362542.1:p.Asp297=