Canonical Allele Identifier: CA1278358964

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907940G= , CM000664.2:g.108907940G=	GRCh38
NC_000002.11:g.109524396G= , CM000664.1:g.109524396G=	GRCh37
NC_000002.10:g.108890828G=	NCBI36
NG_008257.1:g.86433C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.883C= (EDAR) MANE Select	ENSP00000258443.2:p.Gln295=
ENST00000258443.6:c.883C= (EDAR)	ENSP00000258443.2:p.Gln295=
ENST00000376651.1:c.979C= (EDAR)	ENSP00000365839.1:p.Gln327=
ENST00000409271.5:c.979C= (EDAR)	ENSP00000386371.1:p.Gln327=
NM_022336.3:c.883C= (EDAR)	NP_071731.1:p.Gln295=
XM_006712204.1:c.979C= (EDAR)	XP_006712267.1:p.Gln327=
XM_011510502.1:c.1030C= (EDAR)	XP_011508804.1:p.Gln344=
XM_011510503.1:c.934C= (EDAR)	XP_011508805.1:p.Gln312=
XM_011510504.1:c.310C= (EDAR)	XP_011508806.1:p.Gln104=
XM_011510502.2:c.1123C= (EDAR)	XP_011508804.2:p.Gln375=
XM_011510503.2:c.1027C= (EDAR)	XP_011508805.2:p.Gln343=
XM_017004623.2:c.8370+134894G= (RANBP2)	XP_016860112.1:n.8370+134894G=
NM_022336.4:c.883C= (EDAR) MANE Select	NP_071731.1:p.Gln295=