Canonical Allele Identifier: CA1286883888

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127427219C= , CM000664.2:g.127427219C=	GRCh38
NC_000002.11:g.128184795C= , CM000664.1:g.128184795C=	GRCh37
NC_000002.10:g.127901265C=	NCBI36
NG_016323.1:g.13800C= , LRG_599:g.13800C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000312.4:c.793C= MANE Select	NP_000303.1:p.Leu265=
ENST00000234071.8:c.793C= MANE Select	ENSP00000234071.4:p.Leu265=
NM_000312.3:c.793C= , LRG_599t1:c.793C=	NP_000303.1:p.Leu265=
NM_001375602.1:c.976C=	NP_001362531.1:p.Leu326=
NM_001375603.1:c.958C=	NP_001362532.1:p.Leu320=
NM_001375604.1:c.856C=	NP_001362533.1:p.Leu286=
NM_001375605.1:c.895C=	NP_001362534.1:p.Leu299=
NM_001375606.1:c.961C=	NP_001362535.1:p.Leu321=
NM_001375607.1:c.979C=	NP_001362536.1:p.Leu327=
NM_001375608.1:c.736C=	NP_001362537.1:p.Leu246=
NM_001375609.1:c.769C=	NP_001362538.1:p.Leu257=
NM_001375610.1:c.787C=	NP_001362539.1:p.Leu263=
NM_001375611.1:c.793C=	NP_001362540.1:p.Leu265=
NM_001375613.1:c.793C=	NP_001362542.1:p.Leu265=
ENST00000234071.7:c.793C=	ENSP00000234071.3:p.Leu265=
ENST00000402125.2:c.121-1138C=
ENST00000409048.1:c.895C=	ENSP00000386679.1:p.Leu299=
XM_005263715.3:c.976C=	XP_005263772.1:p.Leu326=
XM_005263716.3:c.958C=	XP_005263773.1:p.Leu320=
XM_005263717.3:c.856C=	XP_005263774.1:p.Leu286=
XM_005263717.4:c.856C=	XP_005263774.1:p.Leu286=
XM_017004505.1:c.1036C=	XP_016859994.1:p.Leu346=
XM_024453002.1:c.1138C=	XP_024308770.1:p.Leu380=
XM_024453003.1:c.1078C=	XP_024308771.1:p.Leu360=
XM_024453004.1:c.976C=	XP_024308772.1:p.Leu326=
XM_024453005.1:c.958C=	XP_024308773.1:p.Leu320=
XM_024453006.1:c.895C=	XP_024308774.1:p.Leu299=
XR_923313.1:n.1486-831G=
XR_923313.2:n.4197-831G=