Canonical Allele Identifier: CA348406729

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186487G>T (hg19) ; chr2:g.127428911G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428911G>T , CM000664.2:g.127428911G>T	GRCh38
NC_000002.11:g.128186487G>T , CM000664.1:g.128186487G>T	GRCh37
NC_000002.10:g.127902957G>T	NCBI36
NG_016323.1:g.15492G>T , LRG_599:g.15492G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.1351G>T MANE Select	ENSP00000234071.4:p.Asp451Tyr
ENST00000234071.7:c.1351G>T	ENSP00000234071.3:p.Asp451Tyr
ENST00000402125.2:c.675G>T
ENST00000409048.1:c.1453G>T	ENSP00000386679.1:p.Asp485Tyr
NM_000312.3:c.1351G>T , LRG_599t1:c.1351G>T	NP_000303.1:p.Asp451Tyr
XM_005263715.3:c.1534G>T	XP_005263772.1:p.Asp512Tyr
XM_005263716.3:c.1516G>T	XP_005263773.1:p.Asp506Tyr
XM_005263717.3:c.1414G>T	XP_005263774.1:p.Asp472Tyr
XR_923313.1:n.1332-647C>A
XM_005263717.4:c.1414G>T	XP_005263774.1:p.Asp472Tyr
XM_017004505.1:c.1594G>T	XP_016859994.1:p.Asp532Tyr
XM_024453002.1:c.1696G>T	XP_024308770.1:p.Asp566Tyr
XM_024453003.1:c.1636G>T	XP_024308771.1:p.Asp546Tyr
XM_024453004.1:c.1534G>T	XP_024308772.1:p.Asp512Tyr
XM_024453005.1:c.1516G>T	XP_024308773.1:p.Asp506Tyr
XM_024453006.1:c.1453G>T	XP_024308774.1:p.Asp485Tyr
XR_001739705.1:n.3607-647C>A
XR_923313.2:n.4043-647C>A
NM_000312.4:c.1351G>T MANE Select	NP_000303.1:p.Asp451Tyr
NM_001375602.1:c.1534G>T	NP_001362531.1:p.Asp512Tyr
NM_001375603.1:c.1516G>T	NP_001362532.1:p.Asp506Tyr
NM_001375604.1:c.1414G>T	NP_001362533.1:p.Asp472Tyr
NM_001375605.1:c.1453G>T	NP_001362534.1:p.Asp485Tyr
NM_001375606.1:c.1519G>T	NP_001362535.1:p.Asp507Tyr
NM_001375607.1:c.1537G>T	NP_001362536.1:p.Asp513Tyr
NM_001375608.1:c.1294G>T	NP_001362537.1:p.Asp432Tyr
NM_001375609.1:c.1327G>T	NP_001362538.1:p.Asp443Tyr
NM_001375610.1:c.1345G>T	NP_001362539.1:p.Asp449Tyr
NM_001375611.1:c.1351G>T	NP_001362540.1:p.Asp451Tyr
NM_001375613.1:c.1351G>T	NP_001362542.1:p.Asp451Tyr