Canonical Allele Identifier: CA1278354299

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897149C= , CM000664.2:g.108897149C=	GRCh38
NC_000002.11:g.109513605C= , CM000664.1:g.109513605C=	GRCh37
NC_000002.10:g.108880037C=	NCBI36
NG_008257.1:g.97224G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1105G= (EDAR) MANE Select	ENSP00000258443.2:p.Ala369=
ENST00000258443.6:c.1105G= (EDAR)	ENSP00000258443.2:p.Ala369=
ENST00000376651.1:c.1201G= (EDAR)	ENSP00000365839.1:p.Ala401=
ENST00000409271.5:c.1201G= (EDAR)	ENSP00000386371.1:p.Ala401=
NM_022336.3:c.1105G= (EDAR)	NP_071731.1:p.Ala369=
XM_006712204.1:c.1201G= (EDAR)	XP_006712267.1:p.Ala401=
XM_011510502.1:c.1252G= (EDAR)	XP_011508804.1:p.Ala418=
XM_011510503.1:c.1156G= (EDAR)	XP_011508805.1:p.Ala386=
XM_011510504.1:c.532G= (EDAR)	XP_011508806.1:p.Ala178=
XM_011510502.2:c.1345G= (EDAR)	XP_011508804.2:p.Ala449=
XM_011510503.2:c.1249G= (EDAR)	XP_011508805.2:p.Ala417=
XM_017004623.2:c.8370+124103C= (RANBP2)	XP_016860112.1:n.8370+124103C=
NM_022336.4:c.1105G= (EDAR) MANE Select	NP_071731.1:p.Ala369=