Canonical Allele Identifier: CA348050708

Gene: EDAR RANBP2

Linked Data

• gnomAD v4: 2-108907865-C-T
• MyVariant Identifiers: chr2:g.109524321C>T (hg19) ; chr2:g.108907865C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907865C>T , CM000664.2:g.108907865C>T	GRCh38
NC_000002.11:g.109524321C>T , CM000664.1:g.109524321C>T	GRCh37
NC_000002.10:g.108890753C>T	NCBI36
NG_008257.1:g.86508G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.958G>A (EDAR) MANE Select	ENSP00000258443.2:p.Ala320Thr
ENST00000258443.6:c.958G>A (EDAR)	ENSP00000258443.2:p.Ala320Thr
ENST00000376651.1:c.1054G>A (EDAR)	ENSP00000365839.1:p.Ala352Thr
ENST00000409271.5:c.1054G>A (EDAR)	ENSP00000386371.1:p.Ala352Thr
NM_022336.3:c.958G>A (EDAR)	NP_071731.1:p.Ala320Thr
XM_006712204.1:c.1054G>A (EDAR)	XP_006712267.1:p.Ala352Thr
XM_011510502.1:c.1105G>A (EDAR)	XP_011508804.1:p.Ala369Thr
XM_011510503.1:c.1009G>A (EDAR)	XP_011508805.1:p.Ala337Thr
XM_011510504.1:c.385G>A (EDAR)	XP_011508806.1:p.Ala129Thr
XM_011510502.2:c.1198G>A (EDAR)	XP_011508804.2:p.Ala400Thr
XM_011510503.2:c.1102G>A (EDAR)	XP_011508805.2:p.Ala368Thr
XM_017004623.2:c.8370+134819C>T (RANBP2)	XP_016860112.1:n.8370+134819C>T
NM_022336.4:c.958G>A (EDAR) MANE Select	NP_071731.1:p.Ala320Thr