Canonical Allele Identifier: CA1278354240

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897025T= , CM000664.2:g.108897025T=	GRCh38
NC_000002.11:g.109513481T= , CM000664.1:g.109513481T=	GRCh37
NC_000002.10:g.108879913T=	NCBI36
NG_008257.1:g.97348A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1229A= (EDAR) MANE Select	ENSP00000258443.2:p.Glu410=
ENST00000258443.6:c.1229A= (EDAR)	ENSP00000258443.2:p.Glu410=
ENST00000376651.1:c.1325A= (EDAR)	ENSP00000365839.1:p.Glu442=
ENST00000409271.5:c.1325A= (EDAR)	ENSP00000386371.1:p.Glu442=
NM_022336.3:c.1229A= (EDAR)	NP_071731.1:p.Glu410=
XM_006712204.1:c.1325A= (EDAR)	XP_006712267.1:p.Glu442=
XM_011510502.1:c.1376A= (EDAR)	XP_011508804.1:p.Glu459=
XM_011510503.1:c.1280A= (EDAR)	XP_011508805.1:p.Glu427=
XM_011510504.1:c.656A= (EDAR)	XP_011508806.1:p.Glu219=
XM_011510502.2:c.1469A= (EDAR)	XP_011508804.2:p.Glu490=
XM_011510503.2:c.1373A= (EDAR)	XP_011508805.2:p.Glu458=
XM_017004623.2:c.8370+123979T= (RANBP2)	XP_016860112.1:n.8370+123979T=
NM_022336.4:c.1229A= (EDAR) MANE Select	NP_071731.1:p.Glu410=