Canonical Allele Identifier: CA1286884556

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428621G= , CM000664.2:g.127428621G=	GRCh38
NC_000002.11:g.128186197G= , CM000664.1:g.128186197G=	GRCh37
NC_000002.10:g.127902667G=	NCBI36
NG_016323.1:g.15202G= , LRG_599:g.15202G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1061G= MANE Select	ENSP00000234071.4:p.Arg354=
ENST00000234071.7:c.1061G=	ENSP00000234071.3:p.Arg354=
ENST00000402125.2:c.385G=
ENST00000409048.1:c.1163G=	ENSP00000386679.1:p.Arg388=
NM_000312.3:c.1061G= , LRG_599t1:c.1061G=	NP_000303.1:p.Arg354=
XM_005263715.3:c.1244G=	XP_005263772.1:p.Arg415=
XM_005263716.3:c.1226G=	XP_005263773.1:p.Arg409=
XM_005263717.3:c.1124G=	XP_005263774.1:p.Arg375=
XR_923313.1:n.1332-357C=
XM_005263717.4:c.1124G=	XP_005263774.1:p.Arg375=
XM_017004505.1:c.1304G=	XP_016859994.1:p.Arg435=
XM_024453002.1:c.1406G=	XP_024308770.1:p.Arg469=
XM_024453003.1:c.1346G=	XP_024308771.1:p.Arg449=
XM_024453004.1:c.1244G=	XP_024308772.1:p.Arg415=
XM_024453005.1:c.1226G=	XP_024308773.1:p.Arg409=
XM_024453006.1:c.1163G=	XP_024308774.1:p.Arg388=
XR_001739705.1:n.3607-357C=
XR_923313.2:n.4043-357C=
NM_000312.4:c.1061G= MANE Select	NP_000303.1:p.Arg354=
NM_001375602.1:c.1244G=	NP_001362531.1:p.Arg415=
NM_001375603.1:c.1226G=	NP_001362532.1:p.Arg409=
NM_001375604.1:c.1124G=	NP_001362533.1:p.Arg375=
NM_001375605.1:c.1163G=	NP_001362534.1:p.Arg388=
NM_001375606.1:c.1229G=	NP_001362535.1:p.Arg410=
NM_001375607.1:c.1247G=	NP_001362536.1:p.Arg416=
NM_001375608.1:c.1004G=	NP_001362537.1:p.Arg335=
NM_001375609.1:c.1037G=	NP_001362538.1:p.Arg346=
NM_001375610.1:c.1055G=	NP_001362539.1:p.Arg352=
NM_001375611.1:c.1061G=	NP_001362540.1:p.Arg354=
NM_001375613.1:c.1061G=	NP_001362542.1:p.Arg354=