Canonical Allele Identifier: CA428871573

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186081A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428505A>C , CM000664.2:g.127428505A>C	GRCh38
NC_000002.11:g.128186081A>C , CM000664.1:g.128186081A>C	GRCh37
NC_000002.10:g.127902551A>C	NCBI36
NG_016323.1:g.15086A>C , LRG_599:g.15086A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.945A>C MANE Select	ENSP00000234071.4:p.Ile315=
ENST00000234071.7:c.945A>C	ENSP00000234071.3:p.Ile315=
ENST00000402125.2:c.269A>C
ENST00000409048.1:c.1047A>C	ENSP00000386679.1:p.Ile349=
NM_000312.3:c.945A>C , LRG_599t1:c.945A>C	NP_000303.1:p.Ile315=
XM_005263715.3:c.1128A>C	XP_005263772.1:p.Ile376=
XM_005263716.3:c.1110A>C	XP_005263773.1:p.Ile370=
XM_005263717.3:c.1008A>C	XP_005263774.1:p.Ile336=
XR_923313.1:n.1332-241T>G
XM_005263717.4:c.1008A>C	XP_005263774.1:p.Ile336=
XM_017004505.1:c.1188A>C	XP_016859994.1:p.Ile396=
XM_024453002.1:c.1290A>C	XP_024308770.1:p.Ile430=
XM_024453003.1:c.1230A>C	XP_024308771.1:p.Ile410=
XM_024453004.1:c.1128A>C	XP_024308772.1:p.Ile376=
XM_024453005.1:c.1110A>C	XP_024308773.1:p.Ile370=
XM_024453006.1:c.1047A>C	XP_024308774.1:p.Ile349=
XR_001739705.1:n.3607-241T>G
XR_923313.2:n.4043-241T>G
NM_000312.4:c.945A>C MANE Select	NP_000303.1:p.Ile315=
NM_001375602.1:c.1128A>C	NP_001362531.1:p.Ile376=
NM_001375603.1:c.1110A>C	NP_001362532.1:p.Ile370=
NM_001375604.1:c.1008A>C	NP_001362533.1:p.Ile336=
NM_001375605.1:c.1047A>C	NP_001362534.1:p.Ile349=
NM_001375606.1:c.1113A>C	NP_001362535.1:p.Ile371=
NM_001375607.1:c.1131A>C	NP_001362536.1:p.Ile377=
NM_001375608.1:c.888A>C	NP_001362537.1:p.Ile296=
NM_001375609.1:c.921A>C	NP_001362538.1:p.Ile307=
NM_001375610.1:c.939A>C	NP_001362539.1:p.Ile313=
NM_001375611.1:c.945A>C	NP_001362540.1:p.Ile315=
NM_001375613.1:c.945A>C	NP_001362542.1:p.Ile315=