Canonical Allele Identifier: CA348400019

Gene: PROC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127423351T>A , CM000664.2:g.127423351T>A	GRCh38
NC_000002.11:g.128180927T>A , CM000664.1:g.128180927T>A	GRCh37
NC_000002.10:g.127897397T>A	NCBI36
NG_016323.1:g.9932T>A , LRG_599:g.9932T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000312.4:c.478T>A MANE Select	NP_000303.1:p.Cys160Ser
ENST00000234071.8:c.478T>A MANE Select	ENSP00000234071.4:p.Cys160Ser
NM_000312.3:c.478T>A , LRG_599t1:c.478T>A	NP_000303.1:p.Cys160Ser
NM_001375602.1:c.661T>A	NP_001362531.1:p.Cys221Ser
NM_001375603.1:c.643T>A	NP_001362532.1:p.Cys215Ser
NM_001375604.1:c.541T>A	NP_001362533.1:p.Cys181Ser
NM_001375605.1:c.580T>A	NP_001362534.1:p.Cys194Ser
NM_001375606.1:c.646T>A	NP_001362535.1:p.Cys216Ser
NM_001375607.1:c.664T>A	NP_001362536.1:p.Cys222Ser
NM_001375608.1:c.421T>A	NP_001362537.1:p.Cys141Ser
NM_001375609.1:c.454T>A	NP_001362538.1:p.Cys152Ser
NM_001375610.1:c.472T>A	NP_001362539.1:p.Cys158Ser
NM_001375611.1:c.478T>A	NP_001362540.1:p.Cys160Ser
NM_001375613.1:c.478T>A	NP_001362542.1:p.Cys160Ser
ENST00000234071.7:c.478T>A	ENSP00000234071.3:p.Cys160Ser
ENST00000402125.2:c.63T>A
ENST00000409048.1:c.580T>A	ENSP00000386679.1:p.Cys194Ser
ENST00000442644.5:c.421T>A	ENSP00000411241.1:p.Cys141Ser
ENST00000464089.1:n.64T>A
XM_005263715.3:c.661T>A	XP_005263772.1:p.Cys221Ser
XM_005263716.3:c.643T>A	XP_005263773.1:p.Cys215Ser
XM_005263717.3:c.541T>A	XP_005263774.1:p.Cys181Ser
XM_005263717.4:c.541T>A	XP_005263774.1:p.Cys181Ser
XM_017004505.1:c.721T>A	XP_016859994.1:p.Cys241Ser
XM_024453002.1:c.823T>A	XP_024308770.1:p.Cys275Ser
XM_024453003.1:c.763T>A	XP_024308771.1:p.Cys255Ser
XM_024453004.1:c.661T>A	XP_024308772.1:p.Cys221Ser
XM_024453005.1:c.643T>A	XP_024308773.1:p.Cys215Ser
XM_024453006.1:c.580T>A	XP_024308774.1:p.Cys194Ser