Canonical Allele Identifier: CA1278354277

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897110C= , CM000664.2:g.108897110C=	GRCh38
NC_000002.11:g.109513566C= , CM000664.1:g.109513566C=	GRCh37
NC_000002.10:g.108879998C=	NCBI36
NG_008257.1:g.97263G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1144G= (EDAR) MANE Select	ENSP00000258443.2:p.Gly382=
ENST00000258443.6:c.1144G= (EDAR)	ENSP00000258443.2:p.Gly382=
ENST00000376651.1:c.1240G= (EDAR)	ENSP00000365839.1:p.Gly414=
ENST00000409271.5:c.1240G= (EDAR)	ENSP00000386371.1:p.Gly414=
NM_022336.3:c.1144G= (EDAR)	NP_071731.1:p.Gly382=
XM_006712204.1:c.1240G= (EDAR)	XP_006712267.1:p.Gly414=
XM_011510502.1:c.1291G= (EDAR)	XP_011508804.1:p.Gly431=
XM_011510503.1:c.1195G= (EDAR)	XP_011508805.1:p.Gly399=
XM_011510504.1:c.571G= (EDAR)	XP_011508806.1:p.Gly191=
XM_011510502.2:c.1384G= (EDAR)	XP_011508804.2:p.Gly462=
XM_011510503.2:c.1288G= (EDAR)	XP_011508805.2:p.Gly430=
XM_017004623.2:c.8370+124064C= (RANBP2)	XP_016860112.1:n.8370+124064C=
NM_022336.4:c.1144G= (EDAR) MANE Select	NP_071731.1:p.Gly382=