Canonical Allele Identifier: CA428204151

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513585G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897129G>A , CM000664.2:g.108897129G>A	GRCh38
NC_000002.11:g.109513585G>A , CM000664.1:g.109513585G>A	GRCh37
NC_000002.10:g.108880017G>A	NCBI36
NG_008257.1:g.97244C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1125C>T (EDAR) MANE Select	ENSP00000258443.2:p.Arg375=
ENST00000258443.6:c.1125C>T (EDAR)	ENSP00000258443.2:p.Arg375=
ENST00000376651.1:c.1221C>T (EDAR)	ENSP00000365839.1:p.Arg407=
ENST00000409271.5:c.1221C>T (EDAR)	ENSP00000386371.1:p.Arg407=
NM_022336.3:c.1125C>T (EDAR)	NP_071731.1:p.Arg375=
XM_006712204.1:c.1221C>T (EDAR)	XP_006712267.1:p.Arg407=
XM_011510502.1:c.1272C>T (EDAR)	XP_011508804.1:p.Arg424=
XM_011510503.1:c.1176C>T (EDAR)	XP_011508805.1:p.Arg392=
XM_011510504.1:c.552C>T (EDAR)	XP_011508806.1:p.Arg184=
XM_011510502.2:c.1365C>T (EDAR)	XP_011508804.2:p.Arg455=
XM_011510503.2:c.1269C>T (EDAR)	XP_011508805.2:p.Arg423=
XM_017004623.2:c.8370+124083G>A (RANBP2)	XP_016860112.1:n.8370+124083G>A
NM_022336.4:c.1125C>T (EDAR) MANE Select	NP_071731.1:p.Arg375=