Canonical Allele Identifier: CA1286883409

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426118T= , CM000664.2:g.127426118T=	GRCh38
NC_000002.11:g.128183694T= , CM000664.1:g.128183694T=	GRCh37
NC_000002.10:g.127900164T=	NCBI36
NG_016323.1:g.12699T= , LRG_599:g.12699T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.569T= MANE Select	ENSP00000234071.4:p.Met190=
ENST00000234071.7:c.569T=	ENSP00000234071.3:p.Met190=
ENST00000402125.2:c.121-2239T=
ENST00000409048.1:c.671T=	ENSP00000386679.1:p.Met224=
ENST00000442644.5:c.512T=	ENSP00000411241.1:p.Met171=
ENST00000464089.1:n.155T=
NM_000312.3:c.569T= , LRG_599t1:c.569T=	NP_000303.1:p.Met190=
XM_005263715.3:c.752T=	XP_005263772.1:p.Met251=
XM_005263716.3:c.734T=	XP_005263773.1:p.Met245=
XM_005263717.3:c.632T=	XP_005263774.1:p.Met211=
XM_005263717.4:c.632T=	XP_005263774.1:p.Met211=
XM_017004505.1:c.812T=	XP_016859994.1:p.Met271=
XM_024453002.1:c.914T=	XP_024308770.1:p.Met305=
XM_024453003.1:c.854T=	XP_024308771.1:p.Met285=
XM_024453004.1:c.752T=	XP_024308772.1:p.Met251=
XM_024453005.1:c.734T=	XP_024308773.1:p.Met245=
XM_024453006.1:c.671T=	XP_024308774.1:p.Met224=
XR_923313.2:n.4467A=
NM_000312.4:c.569T= MANE Select	NP_000303.1:p.Met190=
NM_001375602.1:c.752T=	NP_001362531.1:p.Met251=
NM_001375603.1:c.734T=	NP_001362532.1:p.Met245=
NM_001375604.1:c.632T=	NP_001362533.1:p.Met211=
NM_001375605.1:c.671T=	NP_001362534.1:p.Met224=
NM_001375606.1:c.737T=	NP_001362535.1:p.Met246=
NM_001375607.1:c.755T=	NP_001362536.1:p.Met252=
NM_001375608.1:c.512T=	NP_001362537.1:p.Met171=
NM_001375609.1:c.545T=	NP_001362538.1:p.Met182=
NM_001375610.1:c.563T=	NP_001362539.1:p.Met188=
NM_001375611.1:c.569T=	NP_001362540.1:p.Met190=
NM_001375613.1:c.569T=	NP_001362542.1:p.Met190=