Canonical Allele Identifier: CA1278386635

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108959223T= , CM000664.2:g.108959223T=	GRCh38
NC_000002.11:g.109575679T= , CM000664.1:g.109575679T=	GRCh37
NC_000002.10:g.108942111T=	NCBI36
NG_008257.1:g.35150A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.-18-28191A= (EDAR) MANE Select	ENSP00000258443.2:n.-18-28191A=
ENST00000258443.6:c.-18-28191A= (EDAR)	ENSP00000258443.2:n.-18-28191A=
ENST00000376651.1:c.-18-28191A= (EDAR)	ENSP00000365839.1:n.-18-28191A=
ENST00000409271.5:c.-134-18897A= (EDAR)	ENSP00000386371.1:n.-134-18897A=
NM_022336.3:c.-18-28191A= (EDAR)	NP_071731.1:n.-18-28191A=
XM_006712204.1:c.-18-28191A= (EDAR)	XP_006712267.1:n.-18-28191A=
XM_011510502.1:c.33+6400A= (EDAR)	XP_011508804.1:n.33+6400A=
XM_011510503.1:c.33+6400A= (EDAR)	XP_011508805.1:n.33+6400A=
XM_011510502.2:c.126+6400A= (EDAR)	XP_011508804.2:n.126+6400A=
XM_011510503.2:c.126+6400A= (EDAR)	XP_011508805.2:n.126+6400A=
XM_017004623.2:c.8370+186177T= (RANBP2)	XP_016860112.1:n.8370+186177T=
NM_022336.4:c.-18-28191A= (EDAR) MANE Select	NP_071731.1:n.-18-28191A=