Canonical Allele Identifier: CA1286883460

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426224G= , CM000664.2:g.127426224G=	GRCh38
NC_000002.11:g.128183800G= , CM000664.1:g.128183800G=	GRCh37
NC_000002.10:g.127900270G=	NCBI36
NG_016323.1:g.12805G= , LRG_599:g.12805G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.675G= MANE Select	ENSP00000234071.4:p.Trp225=
ENST00000234071.7:c.675G=	ENSP00000234071.3:p.Trp225=
ENST00000402125.2:c.121-2133G=
ENST00000409048.1:c.777G=	ENSP00000386679.1:p.Trp259=
ENST00000464089.1:n.261G=
NM_000312.3:c.675G= , LRG_599t1:c.675G=	NP_000303.1:p.Trp225=
XM_005263715.3:c.858G=	XP_005263772.1:p.Trp286=
XM_005263716.3:c.840G=	XP_005263773.1:p.Trp280=
XM_005263717.3:c.738G=	XP_005263774.1:p.Trp246=
XM_005263717.4:c.738G=	XP_005263774.1:p.Trp246=
XM_017004505.1:c.918G=	XP_016859994.1:p.Trp306=
XM_024453002.1:c.1020G=	XP_024308770.1:p.Trp340=
XM_024453003.1:c.960G=	XP_024308771.1:p.Trp320=
XM_024453004.1:c.858G=	XP_024308772.1:p.Trp286=
XM_024453005.1:c.840G=	XP_024308773.1:p.Trp280=
XM_024453006.1:c.777G=	XP_024308774.1:p.Trp259=
XR_923313.2:n.4361C=
NM_000312.4:c.675G= MANE Select	NP_000303.1:p.Trp225=
NM_001375602.1:c.858G=	NP_001362531.1:p.Trp286=
NM_001375603.1:c.840G=	NP_001362532.1:p.Trp280=
NM_001375604.1:c.738G=	NP_001362533.1:p.Trp246=
NM_001375605.1:c.777G=	NP_001362534.1:p.Trp259=
NM_001375606.1:c.843G=	NP_001362535.1:p.Trp281=
NM_001375607.1:c.861G=	NP_001362536.1:p.Trp287=
NM_001375608.1:c.618G=	NP_001362537.1:p.Trp206=
NM_001375609.1:c.651G=	NP_001362538.1:p.Trp217=
NM_001375610.1:c.669G=	NP_001362539.1:p.Trp223=
NM_001375611.1:c.675G=	NP_001362540.1:p.Trp225=
NM_001375613.1:c.675G=	NP_001362542.1:p.Trp225=