Canonical Allele Identifier: CA427911940

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109524400G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907944G>A , CM000664.2:g.108907944G>A	GRCh38
NC_000002.11:g.109524400G>A , CM000664.1:g.109524400G>A	GRCh37
NC_000002.10:g.108890832G>A	NCBI36
NG_008257.1:g.86429C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.879C>T (EDAR) MANE Select	ENSP00000258443.2:p.Asp293=
ENST00000258443.6:c.879C>T (EDAR)	ENSP00000258443.2:p.Asp293=
ENST00000376651.1:c.975C>T (EDAR)	ENSP00000365839.1:p.Asp325=
ENST00000409271.5:c.975C>T (EDAR)	ENSP00000386371.1:p.Asp325=
NM_022336.3:c.879C>T (EDAR)	NP_071731.1:p.Asp293=
XM_006712204.1:c.975C>T (EDAR)	XP_006712267.1:p.Asp325=
XM_011510502.1:c.1026C>T (EDAR)	XP_011508804.1:p.Asp342=
XM_011510503.1:c.930C>T (EDAR)	XP_011508805.1:p.Asp310=
XM_011510504.1:c.306C>T (EDAR)	XP_011508806.1:p.Asp102=
XM_011510502.2:c.1119C>T (EDAR)	XP_011508804.2:p.Asp373=
XM_011510503.2:c.1023C>T (EDAR)	XP_011508805.2:p.Asp341=
XM_017004623.2:c.8370+134898G>A (RANBP2)	XP_016860112.1:n.8370+134898G>A
NM_022336.4:c.879C>T (EDAR) MANE Select	NP_071731.1:p.Asp293=