Canonical Allele Identifier: CA356143234

Gene: EVC2

Linked Data

• dbSNP Id: rs1715440514
• MyVariant Identifiers: chr4:g.5620271A>T (hg19) ; chr4:g.5618544A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5618544A>T , CM000666.2:g.5618544A>T	GRCh38
NC_000004.11:g.5620271A>T , CM000666.1:g.5620271A>T	GRCh37
NC_000004.10:g.5671172A>T	NCBI36
NG_015821.1:g.96005T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000344408.10:c.2640T>A MANE Select	ENSP00000342144.5:p.Phe880Leu
ENST00000310917.6:c.2400T>A	ENSP00000311683.2:p.Phe800Leu
ENST00000344408.9:c.2640T>A	ENSP00000342144.5:p.Phe880Leu
ENST00000475313.5:c.2400T>A	ENSP00000431981.1:p.Phe800Leu
ENST00000509670.1:c.*1033T>A	ENSP00000423876.1:n.*1033T>A
NM_001166136.1:c.2400T>A	NP_001159608.1:p.Phe800Leu
NM_147127.4:c.2640T>A	NP_667338.3:p.Phe880Leu
XM_011513392.1:c.2649T>A	XP_011511694.1:p.Phe883Leu
XM_011513393.1:c.2649T>A	XP_011511695.1:p.Phe883Leu
XM_011513394.1:c.2409T>A	XP_011511696.1:p.Phe803Leu
XM_017007736.1:c.2400T>A	XP_016863225.1:p.Phe800Leu
XM_017007737.1:c.2400T>A	XP_016863226.1:p.Phe800Leu
XM_017007738.1:c.2640T>A	XP_016863227.1:p.Phe880Leu
XM_017007739.1:c.960T>A	XP_016863228.1:p.Phe320Leu
XM_024453893.1:c.960T>A	XP_024309661.1:p.Phe320Leu
XR_001741141.1:n.2705T>A
NM_147127.5:c.2640T>A MANE Select	NP_667338.3:p.Phe880Leu
NM_001166136.2:c.2400T>A	NP_001159608.1:p.Phe800Leu