Canonical Allele Identifier: CA348404621

Gene: PROC

Linked Data

• dbSNP Id: rs1573459644
• MyVariant Identifiers: chr2:g.128186022A>C (hg19) ; chr2:g.127428446A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428446A>C , CM000664.2:g.127428446A>C	GRCh38
NC_000002.11:g.128186022A>C , CM000664.1:g.128186022A>C	GRCh37
NC_000002.10:g.127902492A>C	NCBI36
NG_016323.1:g.15027A>C , LRG_599:g.15027A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234071.8:c.886A>C MANE Select	ENSP00000234071.4:p.Thr296Pro
ENST00000234071.7:c.886A>C	ENSP00000234071.3:p.Thr296Pro
ENST00000402125.2:c.210A>C
ENST00000409048.1:c.988A>C	ENSP00000386679.1:p.Thr330Pro
NM_000312.3:c.886A>C , LRG_599t1:c.886A>C	NP_000303.1:p.Thr296Pro
XM_005263715.3:c.1069A>C	XP_005263772.1:p.Thr357Pro
XM_005263716.3:c.1051A>C	XP_005263773.1:p.Thr351Pro
XM_005263717.3:c.949A>C	XP_005263774.1:p.Thr317Pro
XR_923313.1:n.1332-182T>G
XM_005263717.4:c.949A>C	XP_005263774.1:p.Thr317Pro
XM_017004505.1:c.1129A>C	XP_016859994.1:p.Thr377Pro
XM_024453002.1:c.1231A>C	XP_024308770.1:p.Thr411Pro
XM_024453003.1:c.1171A>C	XP_024308771.1:p.Thr391Pro
XM_024453004.1:c.1069A>C	XP_024308772.1:p.Thr357Pro
XM_024453005.1:c.1051A>C	XP_024308773.1:p.Thr351Pro
XM_024453006.1:c.988A>C	XP_024308774.1:p.Thr330Pro
XR_001739705.1:n.3607-182T>G
XR_923313.2:n.4043-182T>G
NM_000312.4:c.886A>C MANE Select	NP_000303.1:p.Thr296Pro
NM_001375602.1:c.1069A>C	NP_001362531.1:p.Thr357Pro
NM_001375603.1:c.1051A>C	NP_001362532.1:p.Thr351Pro
NM_001375604.1:c.949A>C	NP_001362533.1:p.Thr317Pro
NM_001375605.1:c.988A>C	NP_001362534.1:p.Thr330Pro
NM_001375606.1:c.1054A>C	NP_001362535.1:p.Thr352Pro
NM_001375607.1:c.1072A>C	NP_001362536.1:p.Thr358Pro
NM_001375608.1:c.829A>C	NP_001362537.1:p.Thr277Pro
NM_001375609.1:c.862A>C	NP_001362538.1:p.Thr288Pro
NM_001375610.1:c.880A>C	NP_001362539.1:p.Thr294Pro
NM_001375611.1:c.886A>C	NP_001362540.1:p.Thr296Pro
NM_001375613.1:c.886A>C	NP_001362542.1:p.Thr296Pro