Canonical Allele Identifier: CA348047631

Gene: EDAR RANBP2

Linked Data

• dbSNP Id: rs1244221558
• gnomAD v2: 2-109513424-G-A
• gnomAD v4: 2-108896968-G-A
• MyVariant Identifiers: chr2:g.109513424G>A (hg19) ; chr2:g.108896968G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108896968G>A , CM000664.2:g.108896968G>A	GRCh38
NC_000002.11:g.109513424G>A , CM000664.1:g.109513424G>A	GRCh37
NC_000002.10:g.108879856G>A	NCBI36
NG_008257.1:g.97405C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1286C>T (EDAR) MANE Select	ENSP00000258443.2:p.Ala429Val
ENST00000258443.6:c.1286C>T (EDAR)	ENSP00000258443.2:p.Ala429Val
ENST00000376651.1:c.1382C>T (EDAR)	ENSP00000365839.1:p.Ala461Val
ENST00000409271.5:c.1382C>T (EDAR)	ENSP00000386371.1:p.Ala461Val
NM_022336.3:c.1286C>T (EDAR)	NP_071731.1:p.Ala429Val
XM_006712204.1:c.1382C>T (EDAR)	XP_006712267.1:p.Ala461Val
XM_011510502.1:c.1433C>T (EDAR)	XP_011508804.1:p.Ala478Val
XM_011510503.1:c.1337C>T (EDAR)	XP_011508805.1:p.Ala446Val
XM_011510504.1:c.713C>T (EDAR)	XP_011508806.1:p.Ala238Val
XM_011510502.2:c.1526C>T (EDAR)	XP_011508804.2:p.Ala509Val
XM_011510503.2:c.1430C>T (EDAR)	XP_011508805.2:p.Ala477Val
XM_017004623.2:c.8370+123922G>A (RANBP2)	XP_016860112.1:n.8370+123922G>A
NM_022336.4:c.1286C>T (EDAR) MANE Select	NP_071731.1:p.Ala429Val