Canonical Allele Identifier: CA1286883442

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426183C= , CM000664.2:g.127426183C=	GRCh38
NC_000002.11:g.128183759C= , CM000664.1:g.128183759C=	GRCh37
NC_000002.10:g.127900229C=	NCBI36
NG_016323.1:g.12764C= , LRG_599:g.12764C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.634C= MANE Select	ENSP00000234071.4:p.Leu212=
ENST00000234071.7:c.634C=	ENSP00000234071.3:p.Leu212=
ENST00000402125.2:c.121-2174C=
ENST00000409048.1:c.736C=	ENSP00000386679.1:p.Leu246=
ENST00000464089.1:n.220C=
NM_000312.3:c.634C= , LRG_599t1:c.634C=	NP_000303.1:p.Leu212=
XM_005263715.3:c.817C=	XP_005263772.1:p.Leu273=
XM_005263716.3:c.799C=	XP_005263773.1:p.Leu267=
XM_005263717.3:c.697C=	XP_005263774.1:p.Leu233=
XM_005263717.4:c.697C=	XP_005263774.1:p.Leu233=
XM_017004505.1:c.877C=	XP_016859994.1:p.Leu293=
XM_024453002.1:c.979C=	XP_024308770.1:p.Leu327=
XM_024453003.1:c.919C=	XP_024308771.1:p.Leu307=
XM_024453004.1:c.817C=	XP_024308772.1:p.Leu273=
XM_024453005.1:c.799C=	XP_024308773.1:p.Leu267=
XM_024453006.1:c.736C=	XP_024308774.1:p.Leu246=
XR_923313.2:n.4402G=
NM_000312.4:c.634C= MANE Select	NP_000303.1:p.Leu212=
NM_001375602.1:c.817C=	NP_001362531.1:p.Leu273=
NM_001375603.1:c.799C=	NP_001362532.1:p.Leu267=
NM_001375604.1:c.697C=	NP_001362533.1:p.Leu233=
NM_001375605.1:c.736C=	NP_001362534.1:p.Leu246=
NM_001375606.1:c.802C=	NP_001362535.1:p.Leu268=
NM_001375607.1:c.820C=	NP_001362536.1:p.Leu274=
NM_001375608.1:c.577C=	NP_001362537.1:p.Leu193=
NM_001375609.1:c.610C=	NP_001362538.1:p.Leu204=
NM_001375610.1:c.628C=	NP_001362539.1:p.Leu210=
NM_001375611.1:c.634C=	NP_001362540.1:p.Leu212=
NM_001375613.1:c.634C=	NP_001362542.1:p.Leu212=