Canonical Allele Identifier: CA438204925

Gene: EVC2

Linked Data

• gnomAD v4: 4-5628570-C-T
• MyVariant Identifiers: chr4:g.5630297C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.5628570C>T , CM000666.2:g.5628570C>T	GRCh38
NC_000004.11:g.5630297C>T , CM000666.1:g.5630297C>T	GRCh37
NC_000004.10:g.5681198C>T	NCBI36
NG_015821.1:g.85979G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344408.10:c.1875G>A MANE Select	ENSP00000342144.5:p.Gln625=
ENST00000310917.6:c.1635G>A	ENSP00000311683.2:p.Gln545=
ENST00000344408.9:c.1875G>A	ENSP00000342144.5:p.Gln625=
ENST00000475313.5:c.1635G>A	ENSP00000431981.1:p.Gln545=
ENST00000509670.1:c.*268G>A	ENSP00000423876.1:n.*268G>A
NM_001166136.1:c.1635G>A	NP_001159608.1:p.Gln545=
NM_147127.4:c.1875G>A	NP_667338.3:p.Gln625=
XM_011513392.1:c.1884G>A	XP_011511694.1:p.Gln628=
XM_011513393.1:c.1884G>A	XP_011511695.1:p.Gln628=
XM_011513394.1:c.1644G>A	XP_011511696.1:p.Gln548=
XM_017007736.1:c.1635G>A	XP_016863225.1:p.Gln545=
XM_017007737.1:c.1635G>A	XP_016863226.1:p.Gln545=
XM_017007738.1:c.1875G>A	XP_016863227.1:p.Gln625=
XM_017007739.1:c.195G>A	XP_016863228.1:p.Gln65=
XM_024453893.1:c.195G>A	XP_024309661.1:p.Gln65=
XR_001741141.1:n.1940G>A
NM_147127.5:c.1875G>A MANE Select	NP_667338.3:p.Gln625=
NM_001166136.2:c.1635G>A	NP_001159608.1:p.Gln545=