Canonical Allele Identifier: CA427911781

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109524325C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907869C>T , CM000664.2:g.108907869C>T	GRCh38
NC_000002.11:g.109524325C>T , CM000664.1:g.109524325C>T	GRCh37
NC_000002.10:g.108890757C>T	NCBI36
NG_008257.1:g.86504G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.954G>A (EDAR) MANE Select	ENSP00000258443.2:p.Lys318=
ENST00000258443.6:c.954G>A (EDAR)	ENSP00000258443.2:p.Lys318=
ENST00000376651.1:c.1050G>A (EDAR)	ENSP00000365839.1:p.Lys350=
ENST00000409271.5:c.1050G>A (EDAR)	ENSP00000386371.1:p.Lys350=
NM_022336.3:c.954G>A (EDAR)	NP_071731.1:p.Lys318=
XM_006712204.1:c.1050G>A (EDAR)	XP_006712267.1:p.Lys350=
XM_011510502.1:c.1101G>A (EDAR)	XP_011508804.1:p.Lys367=
XM_011510503.1:c.1005G>A (EDAR)	XP_011508805.1:p.Lys335=
XM_011510504.1:c.381G>A (EDAR)	XP_011508806.1:p.Lys127=
XM_011510502.2:c.1194G>A (EDAR)	XP_011508804.2:p.Lys398=
XM_011510503.2:c.1098G>A (EDAR)	XP_011508805.2:p.Lys366=
XM_017004623.2:c.8370+134823C>T (RANBP2)	XP_016860112.1:n.8370+134823C>T
NM_022336.4:c.954G>A (EDAR) MANE Select	NP_071731.1:p.Lys318=