Canonical Allele Identifier: CA348405700

Gene: PROC

Linked Data

• MyVariant Identifiers: chr2:g.128186208T>A (hg19) ; chr2:g.127428632T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.127428632T>A , CM000664.2:g.127428632T>A	GRCh38
NC_000002.11:g.128186208T>A , CM000664.1:g.128186208T>A	GRCh37
NC_000002.10:g.127902678T>A	NCBI36
NG_016323.1:g.15213T>A , LRG_599:g.15213T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000234071.8:c.1072T>A MANE Select	ENSP00000234071.4:p.Phe358Ile
ENST00000234071.7:c.1072T>A	ENSP00000234071.3:p.Phe358Ile
ENST00000402125.2:c.396T>A
ENST00000409048.1:c.1174T>A	ENSP00000386679.1:p.Phe392Ile
NM_000312.3:c.1072T>A , LRG_599t1:c.1072T>A	NP_000303.1:p.Phe358Ile
XM_005263715.3:c.1255T>A	XP_005263772.1:p.Phe419Ile
XM_005263716.3:c.1237T>A	XP_005263773.1:p.Phe413Ile
XM_005263717.3:c.1135T>A	XP_005263774.1:p.Phe379Ile
XR_923313.1:n.1332-368A>T
XM_005263717.4:c.1135T>A	XP_005263774.1:p.Phe379Ile
XM_017004505.1:c.1315T>A	XP_016859994.1:p.Phe439Ile
XM_024453002.1:c.1417T>A	XP_024308770.1:p.Phe473Ile
XM_024453003.1:c.1357T>A	XP_024308771.1:p.Phe453Ile
XM_024453004.1:c.1255T>A	XP_024308772.1:p.Phe419Ile
XM_024453005.1:c.1237T>A	XP_024308773.1:p.Phe413Ile
XM_024453006.1:c.1174T>A	XP_024308774.1:p.Phe392Ile
XR_001739705.1:n.3607-368A>T
XR_923313.2:n.4043-368A>T
NM_000312.4:c.1072T>A MANE Select	NP_000303.1:p.Phe358Ile
NM_001375602.1:c.1255T>A	NP_001362531.1:p.Phe419Ile
NM_001375603.1:c.1237T>A	NP_001362532.1:p.Phe413Ile
NM_001375604.1:c.1135T>A	NP_001362533.1:p.Phe379Ile
NM_001375605.1:c.1174T>A	NP_001362534.1:p.Phe392Ile
NM_001375606.1:c.1240T>A	NP_001362535.1:p.Phe414Ile
NM_001375607.1:c.1258T>A	NP_001362536.1:p.Phe420Ile
NM_001375608.1:c.1015T>A	NP_001362537.1:p.Phe339Ile
NM_001375609.1:c.1048T>A	NP_001362538.1:p.Phe350Ile
NM_001375610.1:c.1066T>A	NP_001362539.1:p.Phe356Ile
NM_001375611.1:c.1072T>A	NP_001362540.1:p.Phe358Ile
NM_001375613.1:c.1072T>A	NP_001362542.1:p.Phe358Ile