Canonical Allele Identifier: CA348405277

Gene: PROC

Linked Data

• dbSNP Id: rs1484985689
• MyVariant Identifiers: chr2:g.128186127A>T (hg19) ; chr2:g.127428551A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428551A>T , CM000664.2:g.127428551A>T	GRCh38
NC_000002.11:g.128186127A>T , CM000664.1:g.128186127A>T	GRCh37
NC_000002.10:g.127902597A>T	NCBI36
NG_016323.1:g.15132A>T , LRG_599:g.15132A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.991A>T MANE Select	ENSP00000234071.4:p.Asn331Tyr
ENST00000234071.7:c.991A>T	ENSP00000234071.3:p.Asn331Tyr
ENST00000402125.2:c.315A>T
ENST00000409048.1:c.1093A>T	ENSP00000386679.1:p.Asn365Tyr
NM_000312.3:c.991A>T , LRG_599t1:c.991A>T	NP_000303.1:p.Asn331Tyr
XM_005263715.3:c.1174A>T	XP_005263772.1:p.Asn392Tyr
XM_005263716.3:c.1156A>T	XP_005263773.1:p.Asn386Tyr
XM_005263717.3:c.1054A>T	XP_005263774.1:p.Asn352Tyr
XR_923313.1:n.1332-287T>A
XM_005263717.4:c.1054A>T	XP_005263774.1:p.Asn352Tyr
XM_017004505.1:c.1234A>T	XP_016859994.1:p.Asn412Tyr
XM_024453002.1:c.1336A>T	XP_024308770.1:p.Asn446Tyr
XM_024453003.1:c.1276A>T	XP_024308771.1:p.Asn426Tyr
XM_024453004.1:c.1174A>T	XP_024308772.1:p.Asn392Tyr
XM_024453005.1:c.1156A>T	XP_024308773.1:p.Asn386Tyr
XM_024453006.1:c.1093A>T	XP_024308774.1:p.Asn365Tyr
XR_001739705.1:n.3607-287T>A
XR_923313.2:n.4043-287T>A
NM_000312.4:c.991A>T MANE Select	NP_000303.1:p.Asn331Tyr
NM_001375602.1:c.1174A>T	NP_001362531.1:p.Asn392Tyr
NM_001375603.1:c.1156A>T	NP_001362532.1:p.Asn386Tyr
NM_001375604.1:c.1054A>T	NP_001362533.1:p.Asn352Tyr
NM_001375605.1:c.1093A>T	NP_001362534.1:p.Asn365Tyr
NM_001375606.1:c.1159A>T	NP_001362535.1:p.Asn387Tyr
NM_001375607.1:c.1177A>T	NP_001362536.1:p.Asn393Tyr
NM_001375608.1:c.934A>T	NP_001362537.1:p.Asn312Tyr
NM_001375609.1:c.967A>T	NP_001362538.1:p.Asn323Tyr
NM_001375610.1:c.985A>T	NP_001362539.1:p.Asn329Tyr
NM_001375611.1:c.991A>T	NP_001362540.1:p.Asn331Tyr
NM_001375613.1:c.991A>T	NP_001362542.1:p.Asn331Tyr