Canonical Allele Identifier: CA348406602

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186430T>C (hg19) ; chr2:g.127428854T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428854T>C , CM000664.2:g.127428854T>C	GRCh38
NC_000002.11:g.128186430T>C , CM000664.1:g.128186430T>C	GRCh37
NC_000002.10:g.127902900T>C	NCBI36
NG_016323.1:g.15435T>C , LRG_599:g.15435T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1294T>C MANE Select	ENSP00000234071.4:p.Tyr432His
ENST00000234071.7:c.1294T>C	ENSP00000234071.3:p.Tyr432His
ENST00000402125.2:c.618T>C
ENST00000409048.1:c.1396T>C	ENSP00000386679.1:p.Tyr466His
NM_000312.3:c.1294T>C , LRG_599t1:c.1294T>C	NP_000303.1:p.Tyr432His
XM_005263715.3:c.1477T>C	XP_005263772.1:p.Tyr493His
XM_005263716.3:c.1459T>C	XP_005263773.1:p.Tyr487His
XM_005263717.3:c.1357T>C	XP_005263774.1:p.Tyr453His
XR_923313.1:n.1332-590A>G
XM_005263717.4:c.1357T>C	XP_005263774.1:p.Tyr453His
XM_017004505.1:c.1537T>C	XP_016859994.1:p.Tyr513His
XM_024453002.1:c.1639T>C	XP_024308770.1:p.Tyr547His
XM_024453003.1:c.1579T>C	XP_024308771.1:p.Tyr527His
XM_024453004.1:c.1477T>C	XP_024308772.1:p.Tyr493His
XM_024453005.1:c.1459T>C	XP_024308773.1:p.Tyr487His
XM_024453006.1:c.1396T>C	XP_024308774.1:p.Tyr466His
XR_001739705.1:n.3607-590A>G
XR_923313.2:n.4043-590A>G
NM_000312.4:c.1294T>C MANE Select	NP_000303.1:p.Tyr432His
NM_001375602.1:c.1477T>C	NP_001362531.1:p.Tyr493His
NM_001375603.1:c.1459T>C	NP_001362532.1:p.Tyr487His
NM_001375604.1:c.1357T>C	NP_001362533.1:p.Tyr453His
NM_001375605.1:c.1396T>C	NP_001362534.1:p.Tyr466His
NM_001375606.1:c.1462T>C	NP_001362535.1:p.Tyr488His
NM_001375607.1:c.1480T>C	NP_001362536.1:p.Tyr494His
NM_001375608.1:c.1237T>C	NP_001362537.1:p.Tyr413His
NM_001375609.1:c.1270T>C	NP_001362538.1:p.Tyr424His
NM_001375610.1:c.1288T>C	NP_001362539.1:p.Tyr430His
NM_001375611.1:c.1294T>C	NP_001362540.1:p.Tyr432His
NM_001375613.1:c.1294T>C	NP_001362542.1:p.Tyr432His