Canonical Allele Identifier: CA348404234

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128185939A>G (hg19) ; chr2:g.127428363A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428363A>G , CM000664.2:g.127428363A>G	GRCh38
NC_000002.11:g.128185939A>G , CM000664.1:g.128185939A>G	GRCh37
NC_000002.10:g.127902409A>G	NCBI36
NG_016323.1:g.14944A>G , LRG_599:g.14944A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.803A>G MANE Select	ENSP00000234071.4:p.Tyr268Cys
ENST00000234071.7:c.803A>G	ENSP00000234071.3:p.Tyr268Cys
ENST00000402125.2:c.127A>G
ENST00000409048.1:c.905A>G	ENSP00000386679.1:p.Tyr302Cys
NM_000312.3:c.803A>G , LRG_599t1:c.803A>G	NP_000303.1:p.Tyr268Cys
XM_005263715.3:c.986A>G	XP_005263772.1:p.Tyr329Cys
XM_005263716.3:c.968A>G	XP_005263773.1:p.Tyr323Cys
XM_005263717.3:c.866A>G	XP_005263774.1:p.Tyr289Cys
XR_923313.1:n.1332-99T>C
XM_005263717.4:c.866A>G	XP_005263774.1:p.Tyr289Cys
XM_017004505.1:c.1046A>G	XP_016859994.1:p.Tyr349Cys
XM_024453002.1:c.1148A>G	XP_024308770.1:p.Tyr383Cys
XM_024453003.1:c.1088A>G	XP_024308771.1:p.Tyr363Cys
XM_024453004.1:c.986A>G	XP_024308772.1:p.Tyr329Cys
XM_024453005.1:c.968A>G	XP_024308773.1:p.Tyr323Cys
XM_024453006.1:c.905A>G	XP_024308774.1:p.Tyr302Cys
XR_001739705.1:n.3607-99T>C
XR_923313.2:n.4043-99T>C
NM_000312.4:c.803A>G MANE Select	NP_000303.1:p.Tyr268Cys
NM_001375602.1:c.986A>G	NP_001362531.1:p.Tyr329Cys
NM_001375603.1:c.968A>G	NP_001362532.1:p.Tyr323Cys
NM_001375604.1:c.866A>G	NP_001362533.1:p.Tyr289Cys
NM_001375605.1:c.905A>G	NP_001362534.1:p.Tyr302Cys
NM_001375606.1:c.971A>G	NP_001362535.1:p.Tyr324Cys
NM_001375607.1:c.989A>G	NP_001362536.1:p.Tyr330Cys
NM_001375608.1:c.746A>G	NP_001362537.1:p.Tyr249Cys
NM_001375609.1:c.779A>G	NP_001362538.1:p.Tyr260Cys
NM_001375610.1:c.797A>G	NP_001362539.1:p.Tyr266Cys
NM_001375611.1:c.803A>G	NP_001362540.1:p.Tyr268Cys
NM_001375613.1:c.803A>G	NP_001362542.1:p.Tyr268Cys