Canonical Allele Identifier: CA428203942

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513459C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897003C>T , CM000664.2:g.108897003C>T	GRCh38
NC_000002.11:g.109513459C>T , CM000664.1:g.109513459C>T	GRCh37
NC_000002.10:g.108879891C>T	NCBI36
NG_008257.1:g.97370G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.1251G>A (EDAR) MANE Select	ENSP00000258443.2:p.Gln417=
ENST00000258443.6:c.1251G>A (EDAR)	ENSP00000258443.2:p.Gln417=
ENST00000376651.1:c.1347G>A (EDAR)	ENSP00000365839.1:p.Gln449=
ENST00000409271.5:c.1347G>A (EDAR)	ENSP00000386371.1:p.Gln449=
NM_022336.3:c.1251G>A (EDAR)	NP_071731.1:p.Gln417=
XM_006712204.1:c.1347G>A (EDAR)	XP_006712267.1:p.Gln449=
XM_011510502.1:c.1398G>A (EDAR)	XP_011508804.1:p.Gln466=
XM_011510503.1:c.1302G>A (EDAR)	XP_011508805.1:p.Gln434=
XM_011510504.1:c.678G>A (EDAR)	XP_011508806.1:p.Gln226=
XM_011510502.2:c.1491G>A (EDAR)	XP_011508804.2:p.Gln497=
XM_011510503.2:c.1395G>A (EDAR)	XP_011508805.2:p.Gln465=
XM_017004623.2:c.8370+123957C>T (RANBP2)	XP_016860112.1:n.8370+123957C>T
NM_022336.4:c.1251G>A (EDAR) MANE Select	NP_071731.1:p.Gln417=