Canonical Allele Identifier: CA348048182

Gene: EDAR RANBP2

Linked Data

• dbSNP Id: rs1574362024
• gnomAD v4: 2-108897136-G-A
• COSMIC: COSM1005310 ; COSM4874409
• MyVariant Identifiers: chr2:g.109513592G>A (hg19) ; chr2:g.108897136G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897136G>A , CM000664.2:g.108897136G>A	GRCh38
NC_000002.11:g.109513592G>A , CM000664.1:g.109513592G>A	GRCh37
NC_000002.10:g.108880024G>A	NCBI36
NG_008257.1:g.97237C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1118C>T (EDAR) MANE Select	ENSP00000258443.2:p.Thr373Met
ENST00000258443.6:c.1118C>T (EDAR)	ENSP00000258443.2:p.Thr373Met
ENST00000376651.1:c.1214C>T (EDAR)	ENSP00000365839.1:p.Thr405Met
ENST00000409271.5:c.1214C>T (EDAR)	ENSP00000386371.1:p.Thr405Met
NM_022336.3:c.1118C>T (EDAR)	NP_071731.1:p.Thr373Met
XM_006712204.1:c.1214C>T (EDAR)	XP_006712267.1:p.Thr405Met
XM_011510502.1:c.1265C>T (EDAR)	XP_011508804.1:p.Thr422Met
XM_011510503.1:c.1169C>T (EDAR)	XP_011508805.1:p.Thr390Met
XM_011510504.1:c.545C>T (EDAR)	XP_011508806.1:p.Thr182Met
XM_011510502.2:c.1358C>T (EDAR)	XP_011508804.2:p.Thr453Met
XM_011510503.2:c.1262C>T (EDAR)	XP_011508805.2:p.Thr421Met
XM_017004623.2:c.8370+124090G>A (RANBP2)	XP_016860112.1:n.8370+124090G>A
NM_022336.4:c.1118C>T (EDAR) MANE Select	NP_071731.1:p.Thr373Met