Canonical Allele Identifier: CA1286883438

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426178C= , CM000664.2:g.127426178C=	GRCh38
NC_000002.11:g.128183754C= , CM000664.1:g.128183754C=	GRCh37
NC_000002.10:g.127900224C=	NCBI36
NG_016323.1:g.12759C= , LRG_599:g.12759C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.629C= MANE Select	ENSP00000234071.4:p.Pro210=
ENST00000234071.7:c.629C=	ENSP00000234071.3:p.Pro210=
ENST00000402125.2:c.121-2179C=
ENST00000409048.1:c.731C=	ENSP00000386679.1:p.Pro244=
ENST00000464089.1:n.215C=
NM_000312.3:c.629C= , LRG_599t1:c.629C=	NP_000303.1:p.Pro210=
XM_005263715.3:c.812C=	XP_005263772.1:p.Pro271=
XM_005263716.3:c.794C=	XP_005263773.1:p.Pro265=
XM_005263717.3:c.692C=	XP_005263774.1:p.Pro231=
XM_005263717.4:c.692C=	XP_005263774.1:p.Pro231=
XM_017004505.1:c.872C=	XP_016859994.1:p.Pro291=
XM_024453002.1:c.974C=	XP_024308770.1:p.Pro325=
XM_024453003.1:c.914C=	XP_024308771.1:p.Pro305=
XM_024453004.1:c.812C=	XP_024308772.1:p.Pro271=
XM_024453005.1:c.794C=	XP_024308773.1:p.Pro265=
XM_024453006.1:c.731C=	XP_024308774.1:p.Pro244=
XR_923313.2:n.4407G=
NM_000312.4:c.629C= MANE Select	NP_000303.1:p.Pro210=
NM_001375602.1:c.812C=	NP_001362531.1:p.Pro271=
NM_001375603.1:c.794C=	NP_001362532.1:p.Pro265=
NM_001375604.1:c.692C=	NP_001362533.1:p.Pro231=
NM_001375605.1:c.731C=	NP_001362534.1:p.Pro244=
NM_001375606.1:c.797C=	NP_001362535.1:p.Pro266=
NM_001375607.1:c.815C=	NP_001362536.1:p.Pro272=
NM_001375608.1:c.572C=	NP_001362537.1:p.Pro191=
NM_001375609.1:c.605C=	NP_001362538.1:p.Pro202=
NM_001375610.1:c.623C=	NP_001362539.1:p.Pro208=
NM_001375611.1:c.629C=	NP_001362540.1:p.Pro210=
NM_001375613.1:c.629C=	NP_001362542.1:p.Pro210=