Canonical Allele Identifier: CA348405691

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186202C>A (hg19) ; chr2:g.127428626C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428626C>A , CM000664.2:g.127428626C>A	GRCh38
NC_000002.11:g.128186202C>A , CM000664.1:g.128186202C>A	GRCh37
NC_000002.10:g.127902672C>A	NCBI36
NG_016323.1:g.15207C>A , LRG_599:g.15207C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1066C>A MANE Select	ENSP00000234071.4:p.Arg356Ser
ENST00000234071.7:c.1066C>A	ENSP00000234071.3:p.Arg356Ser
ENST00000402125.2:c.390C>A
ENST00000409048.1:c.1168C>A	ENSP00000386679.1:p.Arg390Ser
NM_000312.3:c.1066C>A , LRG_599t1:c.1066C>A	NP_000303.1:p.Arg356Ser
XM_005263715.3:c.1249C>A	XP_005263772.1:p.Arg417Ser
XM_005263716.3:c.1231C>A	XP_005263773.1:p.Arg411Ser
XM_005263717.3:c.1129C>A	XP_005263774.1:p.Arg377Ser
XR_923313.1:n.1332-362G>T
XM_005263717.4:c.1129C>A	XP_005263774.1:p.Arg377Ser
XM_017004505.1:c.1309C>A	XP_016859994.1:p.Arg437Ser
XM_024453002.1:c.1411C>A	XP_024308770.1:p.Arg471Ser
XM_024453003.1:c.1351C>A	XP_024308771.1:p.Arg451Ser
XM_024453004.1:c.1249C>A	XP_024308772.1:p.Arg417Ser
XM_024453005.1:c.1231C>A	XP_024308773.1:p.Arg411Ser
XM_024453006.1:c.1168C>A	XP_024308774.1:p.Arg390Ser
XR_001739705.1:n.3607-362G>T
XR_923313.2:n.4043-362G>T
NM_000312.4:c.1066C>A MANE Select	NP_000303.1:p.Arg356Ser
NM_001375602.1:c.1249C>A	NP_001362531.1:p.Arg417Ser
NM_001375603.1:c.1231C>A	NP_001362532.1:p.Arg411Ser
NM_001375604.1:c.1129C>A	NP_001362533.1:p.Arg377Ser
NM_001375605.1:c.1168C>A	NP_001362534.1:p.Arg390Ser
NM_001375606.1:c.1234C>A	NP_001362535.1:p.Arg412Ser
NM_001375607.1:c.1252C>A	NP_001362536.1:p.Arg418Ser
NM_001375608.1:c.1009C>A	NP_001362537.1:p.Arg337Ser
NM_001375609.1:c.1042C>A	NP_001362538.1:p.Arg348Ser
NM_001375610.1:c.1060C>A	NP_001362539.1:p.Arg354Ser
NM_001375611.1:c.1066C>A	NP_001362540.1:p.Arg356Ser
NM_001375613.1:c.1066C>A	NP_001362542.1:p.Arg356Ser