Canonical Allele Identifier: CA1278365622

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108923197A= , CM000664.2:g.108923197A=	GRCh38
NC_000002.11:g.109539653A= , CM000664.1:g.109539653A=	GRCh37
NC_000002.10:g.108906085A=	NCBI36
NG_008257.1:g.71176T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.442+171T= (EDAR) MANE Select	ENSP00000258443.2:n.442+171T=
ENST00000258443.6:c.442+171T= (EDAR)	ENSP00000258443.2:n.442+171T=
ENST00000376651.1:c.442+171T= (EDAR)	ENSP00000365839.1:n.442+171T=
ENST00000409271.5:c.442+171T= (EDAR)	ENSP00000386371.1:n.442+171T=
NM_022336.3:c.442+171T= (EDAR)	NP_071731.1:n.442+171T=
XM_006712204.1:c.442+171T= (EDAR)	XP_006712267.1:n.442+171T=
XM_011510502.1:c.493+171T= (EDAR)	XP_011508804.1:n.493+171T=
XM_011510503.1:c.493+171T= (EDAR)	XP_011508805.1:n.493+171T=
XM_011510502.2:c.586+171T= (EDAR)	XP_011508804.2:n.586+171T=
XM_011510503.2:c.586+171T= (EDAR)	XP_011508805.2:n.586+171T=
XM_017004623.2:c.8370+150151A= (RANBP2)	XP_016860112.1:n.8370+150151A=
NM_022336.4:c.442+171T= (EDAR) MANE Select	NP_071731.1:n.442+171T=