Canonical Allele Identifier: CA1278358958

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907930G= , CM000664.2:g.108907930G=	GRCh38
NC_000002.11:g.109524386G= , CM000664.1:g.109524386G=	GRCh37
NC_000002.10:g.108890818G=	NCBI36
NG_008257.1:g.86443C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.893C= (EDAR) MANE Select	ENSP00000258443.2:p.Pro298=
ENST00000258443.6:c.893C= (EDAR)	ENSP00000258443.2:p.Pro298=
ENST00000376651.1:c.989C= (EDAR)	ENSP00000365839.1:p.Pro330=
ENST00000409271.5:c.989C= (EDAR)	ENSP00000386371.1:p.Pro330=
NM_022336.3:c.893C= (EDAR)	NP_071731.1:p.Pro298=
XM_006712204.1:c.989C= (EDAR)	XP_006712267.1:p.Pro330=
XM_011510502.1:c.1040C= (EDAR)	XP_011508804.1:p.Pro347=
XM_011510503.1:c.944C= (EDAR)	XP_011508805.1:p.Pro315=
XM_011510504.1:c.320C= (EDAR)	XP_011508806.1:p.Pro107=
XM_011510502.2:c.1133C= (EDAR)	XP_011508804.2:p.Pro378=
XM_011510503.2:c.1037C= (EDAR)	XP_011508805.2:p.Pro346=
XM_017004623.2:c.8370+134884G= (RANBP2)	XP_016860112.1:n.8370+134884G=
NM_022336.4:c.893C= (EDAR) MANE Select	NP_071731.1:p.Pro298=