Canonical Allele Identifier: CA1286884706

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428895C= , CM000664.2:g.127428895C=	GRCh38
NC_000002.11:g.128186471C= , CM000664.1:g.128186471C=	GRCh37
NC_000002.10:g.127902941C=	NCBI36
NG_016323.1:g.15476C= , LRG_599:g.15476C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1335C= MANE Select	ENSP00000234071.4:p.Ile445=
ENST00000234071.7:c.1335C=	ENSP00000234071.3:p.Ile445=
ENST00000402125.2:c.659C=
ENST00000409048.1:c.1437C=	ENSP00000386679.1:p.Ile479=
NM_000312.3:c.1335C= , LRG_599t1:c.1335C=	NP_000303.1:p.Ile445=
XM_005263715.3:c.1518C=	XP_005263772.1:p.Ile506=
XM_005263716.3:c.1500C=	XP_005263773.1:p.Ile500=
XM_005263717.3:c.1398C=	XP_005263774.1:p.Ile466=
XR_923313.1:n.1332-631G=
XM_005263717.4:c.1398C=	XP_005263774.1:p.Ile466=
XM_017004505.1:c.1578C=	XP_016859994.1:p.Ile526=
XM_024453002.1:c.1680C=	XP_024308770.1:p.Ile560=
XM_024453003.1:c.1620C=	XP_024308771.1:p.Ile540=
XM_024453004.1:c.1518C=	XP_024308772.1:p.Ile506=
XM_024453005.1:c.1500C=	XP_024308773.1:p.Ile500=
XM_024453006.1:c.1437C=	XP_024308774.1:p.Ile479=
XR_001739705.1:n.3607-631G=
XR_923313.2:n.4043-631G=
NM_000312.4:c.1335C= MANE Select	NP_000303.1:p.Ile445=
NM_001375602.1:c.1518C=	NP_001362531.1:p.Ile506=
NM_001375603.1:c.1500C=	NP_001362532.1:p.Ile500=
NM_001375604.1:c.1398C=	NP_001362533.1:p.Ile466=
NM_001375605.1:c.1437C=	NP_001362534.1:p.Ile479=
NM_001375606.1:c.1503C=	NP_001362535.1:p.Ile501=
NM_001375607.1:c.1521C=	NP_001362536.1:p.Ile507=
NM_001375608.1:c.1278C=	NP_001362537.1:p.Ile426=
NM_001375609.1:c.1311C=	NP_001362538.1:p.Ile437=
NM_001375610.1:c.1329C=	NP_001362539.1:p.Ile443=
NM_001375611.1:c.1335C=	NP_001362540.1:p.Ile445=
NM_001375613.1:c.1335C=	NP_001362542.1:p.Ile445=