Canonical Allele Identifier: CA348048155

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513578C>G (hg19) ; chr2:g.108897122C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897122C>G , CM000664.2:g.108897122C>G	GRCh38
NC_000002.11:g.109513578C>G , CM000664.1:g.109513578C>G	GRCh37
NC_000002.10:g.108880010C>G	NCBI36
NG_008257.1:g.97251G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1132G>C (EDAR) MANE Select	ENSP00000258443.2:p.Ala378Pro
ENST00000258443.6:c.1132G>C (EDAR)	ENSP00000258443.2:p.Ala378Pro
ENST00000376651.1:c.1228G>C (EDAR)	ENSP00000365839.1:p.Ala410Pro
ENST00000409271.5:c.1228G>C (EDAR)	ENSP00000386371.1:p.Ala410Pro
NM_022336.3:c.1132G>C (EDAR)	NP_071731.1:p.Ala378Pro
XM_006712204.1:c.1228G>C (EDAR)	XP_006712267.1:p.Ala410Pro
XM_011510502.1:c.1279G>C (EDAR)	XP_011508804.1:p.Ala427Pro
XM_011510503.1:c.1183G>C (EDAR)	XP_011508805.1:p.Ala395Pro
XM_011510504.1:c.559G>C (EDAR)	XP_011508806.1:p.Ala187Pro
XM_011510502.2:c.1372G>C (EDAR)	XP_011508804.2:p.Ala458Pro
XM_011510503.2:c.1276G>C (EDAR)	XP_011508805.2:p.Ala426Pro
XM_017004623.2:c.8370+124076C>G (RANBP2)	XP_016860112.1:n.8370+124076C>G
NM_022336.4:c.1132G>C (EDAR) MANE Select	NP_071731.1:p.Ala378Pro