Canonical Allele Identifier: CA1824821

Gene: EDAR RANBP2

Linked Data

• dbSNP Id: rs201979277
• ExAC: 2:109513622 G / T
• gnomAD v2: 2-109513622-G-T
• MyVariant Identifiers: chr2:g.109513622G>T (hg19) ; chr2:g.108897166G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897166G>T , CM000664.2:g.108897166G>T	GRCh38
NC_000002.11:g.109513622G>T , CM000664.1:g.109513622G>T	GRCh37
NC_000002.10:g.108880054G>T	NCBI36
NG_008257.1:g.97207C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1088C>A (EDAR) MANE Select	ENSP00000258443.2:p.Thr363Lys
ENST00000258443.6:c.1088C>A (EDAR)	ENSP00000258443.2:p.Thr363Lys
ENST00000376651.1:c.1184C>A (EDAR)	ENSP00000365839.1:p.Thr395Lys
ENST00000409271.5:c.1184C>A (EDAR)	ENSP00000386371.1:p.Thr395Lys
NM_022336.3:c.1088C>A (EDAR)	NP_071731.1:p.Thr363Lys
XM_006712204.1:c.1184C>A (EDAR)	XP_006712267.1:p.Thr395Lys
XM_011510502.1:c.1235C>A (EDAR)	XP_011508804.1:p.Thr412Lys
XM_011510503.1:c.1139C>A (EDAR)	XP_011508805.1:p.Thr380Lys
XM_011510504.1:c.515C>A (EDAR)	XP_011508806.1:p.Thr172Lys
XM_011510502.2:c.1328C>A (EDAR)	XP_011508804.2:p.Thr443Lys
XM_011510503.2:c.1232C>A (EDAR)	XP_011508805.2:p.Thr411Lys
XM_017004623.2:c.8370+124120G>T (RANBP2)	XP_016860112.1:n.8370+124120G>T
NM_022336.4:c.1088C>A (EDAR) MANE Select	NP_071731.1:p.Thr363Lys