Canonical Allele Identifier: CA1286883445

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426191T= , CM000664.2:g.127426191T=	GRCh38
NC_000002.11:g.128183767T= , CM000664.1:g.128183767T=	GRCh37
NC_000002.10:g.127900237T=	NCBI36
NG_016323.1:g.12772T= , LRG_599:g.12772T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.642T= MANE Select	ENSP00000234071.4:p.Asp214=
ENST00000234071.7:c.642T=	ENSP00000234071.3:p.Asp214=
ENST00000402125.2:c.121-2166T=
ENST00000409048.1:c.744T=	ENSP00000386679.1:p.Asp248=
ENST00000464089.1:n.228T=
NM_000312.3:c.642T= , LRG_599t1:c.642T=	NP_000303.1:p.Asp214=
XM_005263715.3:c.825T=	XP_005263772.1:p.Asp275=
XM_005263716.3:c.807T=	XP_005263773.1:p.Asp269=
XM_005263717.3:c.705T=	XP_005263774.1:p.Asp235=
XM_005263717.4:c.705T=	XP_005263774.1:p.Asp235=
XM_017004505.1:c.885T=	XP_016859994.1:p.Asp295=
XM_024453002.1:c.987T=	XP_024308770.1:p.Asp329=
XM_024453003.1:c.927T=	XP_024308771.1:p.Asp309=
XM_024453004.1:c.825T=	XP_024308772.1:p.Asp275=
XM_024453005.1:c.807T=	XP_024308773.1:p.Asp269=
XM_024453006.1:c.744T=	XP_024308774.1:p.Asp248=
XR_923313.2:n.4394A=
NM_000312.4:c.642T= MANE Select	NP_000303.1:p.Asp214=
NM_001375602.1:c.825T=	NP_001362531.1:p.Asp275=
NM_001375603.1:c.807T=	NP_001362532.1:p.Asp269=
NM_001375604.1:c.705T=	NP_001362533.1:p.Asp235=
NM_001375605.1:c.744T=	NP_001362534.1:p.Asp248=
NM_001375606.1:c.810T=	NP_001362535.1:p.Asp270=
NM_001375607.1:c.828T=	NP_001362536.1:p.Asp276=
NM_001375608.1:c.585T=	NP_001362537.1:p.Asp195=
NM_001375609.1:c.618T=	NP_001362538.1:p.Asp206=
NM_001375610.1:c.636T=	NP_001362539.1:p.Asp212=
NM_001375611.1:c.642T=	NP_001362540.1:p.Asp214=
NM_001375613.1:c.642T=	NP_001362542.1:p.Asp214=