Canonical Allele Identifier: CA1278359083

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108908173G= , CM000664.2:g.108908173G=	GRCh38
NC_000002.11:g.109524629G= , CM000664.1:g.109524629G=	GRCh37
NC_000002.10:g.108891061G=	NCBI36
NG_008257.1:g.86200C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.804-154C= (EDAR) MANE Select	ENSP00000258443.2:n.804-154C=
ENST00000258443.6:c.804-154C= (EDAR)	ENSP00000258443.2:n.804-154C=
ENST00000376651.1:c.900-154C= (EDAR)	ENSP00000365839.1:n.900-154C=
ENST00000409271.5:c.900-154C= (EDAR)	ENSP00000386371.1:n.900-154C=
NM_022336.3:c.804-154C= (EDAR)	NP_071731.1:n.804-154C=
XM_006712204.1:c.900-154C= (EDAR)	XP_006712267.1:n.900-154C=
XM_011510502.1:c.951-154C= (EDAR)	XP_011508804.1:n.951-154C=
XM_011510503.1:c.855-154C= (EDAR)	XP_011508805.1:n.855-154C=
XM_011510504.1:c.231-154C= (EDAR)	XP_011508806.1:n.231-154C=
XM_011510502.2:c.1044-154C= (EDAR)	XP_011508804.2:n.1044-154C=
XM_011510503.2:c.948-154C= (EDAR)	XP_011508805.2:n.948-154C=
XM_017004623.2:c.8370+135127G= (RANBP2)	XP_016860112.1:n.8370+135127G=
NM_022336.4:c.804-154C= (EDAR) MANE Select	NP_071731.1:n.804-154C=