Canonical Allele Identifier: CA1286883449

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426208G= , CM000664.2:g.127426208G=	GRCh38
NC_000002.11:g.128183784G= , CM000664.1:g.128183784G=	GRCh37
NC_000002.10:g.127900254G=	NCBI36
NG_016323.1:g.12789G= , LRG_599:g.12789G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.659G= MANE Select	ENSP00000234071.4:p.Arg220=
ENST00000234071.7:c.659G=	ENSP00000234071.3:p.Arg220=
ENST00000402125.2:c.121-2149G=
ENST00000409048.1:c.761G=	ENSP00000386679.1:p.Arg254=
ENST00000464089.1:n.245G=
NM_000312.3:c.659G= , LRG_599t1:c.659G=	NP_000303.1:p.Arg220=
XM_005263715.3:c.842G=	XP_005263772.1:p.Arg281=
XM_005263716.3:c.824G=	XP_005263773.1:p.Arg275=
XM_005263717.3:c.722G=	XP_005263774.1:p.Arg241=
XM_005263717.4:c.722G=	XP_005263774.1:p.Arg241=
XM_017004505.1:c.902G=	XP_016859994.1:p.Arg301=
XM_024453002.1:c.1004G=	XP_024308770.1:p.Arg335=
XM_024453003.1:c.944G=	XP_024308771.1:p.Arg315=
XM_024453004.1:c.842G=	XP_024308772.1:p.Arg281=
XM_024453005.1:c.824G=	XP_024308773.1:p.Arg275=
XM_024453006.1:c.761G=	XP_024308774.1:p.Arg254=
XR_923313.2:n.4377C=
NM_000312.4:c.659G= MANE Select	NP_000303.1:p.Arg220=
NM_001375602.1:c.842G=	NP_001362531.1:p.Arg281=
NM_001375603.1:c.824G=	NP_001362532.1:p.Arg275=
NM_001375604.1:c.722G=	NP_001362533.1:p.Arg241=
NM_001375605.1:c.761G=	NP_001362534.1:p.Arg254=
NM_001375606.1:c.827G=	NP_001362535.1:p.Arg276=
NM_001375607.1:c.845G=	NP_001362536.1:p.Arg282=
NM_001375608.1:c.602G=	NP_001362537.1:p.Arg201=
NM_001375609.1:c.635G=	NP_001362538.1:p.Arg212=
NM_001375610.1:c.653G=	NP_001362539.1:p.Arg218=
NM_001375611.1:c.659G=	NP_001362540.1:p.Arg220=
NM_001375613.1:c.659G=	NP_001362542.1:p.Arg220=