Canonical Allele Identifier: CA348401058

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128183684T>C (hg19) ; chr2:g.127426108T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127426108T>C , CM000664.2:g.127426108T>C	GRCh38
NC_000002.11:g.128183684T>C , CM000664.1:g.128183684T>C	GRCh37
NC_000002.10:g.127900154T>C	NCBI36
NG_016323.1:g.12689T>C , LRG_599:g.12689T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.559T>C MANE Select	ENSP00000234071.4:p.Trp187Arg
ENST00000234071.7:c.559T>C	ENSP00000234071.3:p.Trp187Arg
ENST00000402125.2:c.121-2249T>C
ENST00000409048.1:c.661T>C	ENSP00000386679.1:p.Trp221Arg
ENST00000442644.5:c.502T>C	ENSP00000411241.1:p.Trp168Arg
ENST00000464089.1:n.145T>C
NM_000312.3:c.559T>C , LRG_599t1:c.559T>C	NP_000303.1:p.Trp187Arg
XM_005263715.3:c.742T>C	XP_005263772.1:p.Trp248Arg
XM_005263716.3:c.724T>C	XP_005263773.1:p.Trp242Arg
XM_005263717.3:c.622T>C	XP_005263774.1:p.Trp208Arg
XM_005263717.4:c.622T>C	XP_005263774.1:p.Trp208Arg
XM_017004505.1:c.802T>C	XP_016859994.1:p.Trp268Arg
XM_024453002.1:c.904T>C	XP_024308770.1:p.Trp302Arg
XM_024453003.1:c.844T>C	XP_024308771.1:p.Trp282Arg
XM_024453004.1:c.742T>C	XP_024308772.1:p.Trp248Arg
XM_024453005.1:c.724T>C	XP_024308773.1:p.Trp242Arg
XM_024453006.1:c.661T>C	XP_024308774.1:p.Trp221Arg
XR_923313.2:n.4477A>G
NM_000312.4:c.559T>C MANE Select	NP_000303.1:p.Trp187Arg
NM_001375602.1:c.742T>C	NP_001362531.1:p.Trp248Arg
NM_001375603.1:c.724T>C	NP_001362532.1:p.Trp242Arg
NM_001375604.1:c.622T>C	NP_001362533.1:p.Trp208Arg
NM_001375605.1:c.661T>C	NP_001362534.1:p.Trp221Arg
NM_001375606.1:c.727T>C	NP_001362535.1:p.Trp243Arg
NM_001375607.1:c.745T>C	NP_001362536.1:p.Trp249Arg
NM_001375608.1:c.502T>C	NP_001362537.1:p.Trp168Arg
NM_001375609.1:c.535T>C	NP_001362538.1:p.Trp179Arg
NM_001375610.1:c.553T>C	NP_001362539.1:p.Trp185Arg
NM_001375611.1:c.559T>C	NP_001362540.1:p.Trp187Arg
NM_001375613.1:c.559T>C	NP_001362542.1:p.Trp187Arg