Canonical Allele Identifier: CA1278360134

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108910459C= , CM000664.2:g.108910459C=	GRCh38
NC_000002.11:g.109526915C= , CM000664.1:g.109526915C=	GRCh37
NC_000002.10:g.108893347C=	NCBI36
NG_008257.1:g.83914G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.803+1G= (EDAR) MANE Select	ENSP00000258443.2:n.803+1G=
ENST00000258443.6:c.803+1G= (EDAR)	ENSP00000258443.2:n.803+1G=
ENST00000376651.1:c.899+1G= (EDAR)	ENSP00000365839.1:n.899+1G=
ENST00000409271.5:c.899+1G= (EDAR)	ENSP00000386371.1:n.899+1G=
NM_022336.3:c.803+1G= (EDAR)	NP_071731.1:n.803+1G=
XM_006712204.1:c.899+1G= (EDAR)	XP_006712267.1:n.899+1G=
XM_011510502.1:c.950+1G= (EDAR)	XP_011508804.1:n.950+1G=
XM_011510503.1:c.854+1G= (EDAR)	XP_011508805.1:n.854+1G=
XM_011510504.1:c.230+1G= (EDAR)	XP_011508806.1:n.230+1G=
XM_011510502.2:c.1043+1G= (EDAR)	XP_011508804.2:n.1043+1G=
XM_011510503.2:c.947+1G= (EDAR)	XP_011508805.2:n.947+1G=
XM_017004623.2:c.8370+137413C= (RANBP2)	XP_016860112.1:n.8370+137413C=
NM_022336.4:c.803+1G= (EDAR) MANE Select	NP_071731.1:n.803+1G=