Canonical Allele Identifier: CA348406487

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186398G>C (hg19) ; chr2:g.127428822G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428822G>C , CM000664.2:g.127428822G>C	GRCh38
NC_000002.11:g.128186398G>C , CM000664.1:g.128186398G>C	GRCh37
NC_000002.10:g.127902868G>C	NCBI36
NG_016323.1:g.15403G>C , LRG_599:g.15403G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1262G>C MANE Select	ENSP00000234071.4:p.Ser421Thr
ENST00000234071.7:c.1262G>C	ENSP00000234071.3:p.Ser421Thr
ENST00000402125.2:c.586G>C
ENST00000409048.1:c.1364G>C	ENSP00000386679.1:p.Ser455Thr
NM_000312.3:c.1262G>C , LRG_599t1:c.1262G>C	NP_000303.1:p.Ser421Thr
XM_005263715.3:c.1445G>C	XP_005263772.1:p.Ser482Thr
XM_005263716.3:c.1427G>C	XP_005263773.1:p.Ser476Thr
XM_005263717.3:c.1325G>C	XP_005263774.1:p.Ser442Thr
XR_923313.1:n.1332-558C>G
XM_005263717.4:c.1325G>C	XP_005263774.1:p.Ser442Thr
XM_017004505.1:c.1505G>C	XP_016859994.1:p.Ser502Thr
XM_024453002.1:c.1607G>C	XP_024308770.1:p.Ser536Thr
XM_024453003.1:c.1547G>C	XP_024308771.1:p.Ser516Thr
XM_024453004.1:c.1445G>C	XP_024308772.1:p.Ser482Thr
XM_024453005.1:c.1427G>C	XP_024308773.1:p.Ser476Thr
XM_024453006.1:c.1364G>C	XP_024308774.1:p.Ser455Thr
XR_001739705.1:n.3607-558C>G
XR_923313.2:n.4043-558C>G
NM_000312.4:c.1262G>C MANE Select	NP_000303.1:p.Ser421Thr
NM_001375602.1:c.1445G>C	NP_001362531.1:p.Ser482Thr
NM_001375603.1:c.1427G>C	NP_001362532.1:p.Ser476Thr
NM_001375604.1:c.1325G>C	NP_001362533.1:p.Ser442Thr
NM_001375605.1:c.1364G>C	NP_001362534.1:p.Ser455Thr
NM_001375606.1:c.1430G>C	NP_001362535.1:p.Ser477Thr
NM_001375607.1:c.1448G>C	NP_001362536.1:p.Ser483Thr
NM_001375608.1:c.1205G>C	NP_001362537.1:p.Ser402Thr
NM_001375609.1:c.1238G>C	NP_001362538.1:p.Ser413Thr
NM_001375610.1:c.1256G>C	NP_001362539.1:p.Ser419Thr
NM_001375611.1:c.1262G>C	NP_001362540.1:p.Ser421Thr
NM_001375613.1:c.1262G>C	NP_001362542.1:p.Ser421Thr