Canonical Allele Identifier: CA1278354195

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108896923G= , CM000664.2:g.108896923G=	GRCh38
NC_000002.11:g.109513379G= , CM000664.1:g.109513379G=	GRCh37
NC_000002.10:g.108879811G=	NCBI36
NG_008257.1:g.97450C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.1331C= (EDAR) MANE Select	ENSP00000258443.2:p.Pro444=
ENST00000258443.6:c.1331C= (EDAR)	ENSP00000258443.2:p.Pro444=
ENST00000376651.1:c.1427C= (EDAR)	ENSP00000365839.1:p.Pro476=
ENST00000409271.5:c.1427C= (EDAR)	ENSP00000386371.1:p.Pro476=
NM_022336.3:c.1331C= (EDAR)	NP_071731.1:p.Pro444=
XM_006712204.1:c.1427C= (EDAR)	XP_006712267.1:p.Pro476=
XM_011510502.1:c.1478C= (EDAR)	XP_011508804.1:p.Pro493=
XM_011510503.1:c.1382C= (EDAR)	XP_011508805.1:p.Pro461=
XM_011510504.1:c.758C= (EDAR)	XP_011508806.1:p.Pro253=
XM_011510502.2:c.1571C= (EDAR)	XP_011508804.2:p.Pro524=
XM_011510503.2:c.1475C= (EDAR)	XP_011508805.2:p.Pro492=
XM_017004623.2:c.8370+123877G= (RANBP2)	XP_016860112.1:n.8370+123877G=
NM_022336.4:c.1331C= (EDAR) MANE Select	NP_071731.1:p.Pro444=