Canonical Allele Identifier: CA348047639

Gene: EDAR RANBP2

Linked Data

• gnomAD v4: 2-108896969-C-T
• MyVariant Identifiers: chr2:g.109513425C>T (hg19) ; chr2:g.108896969C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108896969C>T , CM000664.2:g.108896969C>T	GRCh38
NC_000002.11:g.109513425C>T , CM000664.1:g.109513425C>T	GRCh37
NC_000002.10:g.108879857C>T	NCBI36
NG_008257.1:g.97404G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.1285G>A (EDAR) MANE Select	ENSP00000258443.2:p.Ala429Thr
ENST00000258443.6:c.1285G>A (EDAR)	ENSP00000258443.2:p.Ala429Thr
ENST00000376651.1:c.1381G>A (EDAR)	ENSP00000365839.1:p.Ala461Thr
ENST00000409271.5:c.1381G>A (EDAR)	ENSP00000386371.1:p.Ala461Thr
NM_022336.3:c.1285G>A (EDAR)	NP_071731.1:p.Ala429Thr
XM_006712204.1:c.1381G>A (EDAR)	XP_006712267.1:p.Ala461Thr
XM_011510502.1:c.1432G>A (EDAR)	XP_011508804.1:p.Ala478Thr
XM_011510503.1:c.1336G>A (EDAR)	XP_011508805.1:p.Ala446Thr
XM_011510504.1:c.712G>A (EDAR)	XP_011508806.1:p.Ala238Thr
XM_011510502.2:c.1525G>A (EDAR)	XP_011508804.2:p.Ala509Thr
XM_011510503.2:c.1429G>A (EDAR)	XP_011508805.2:p.Ala477Thr
XM_017004623.2:c.8370+123923C>T (RANBP2)	XP_016860112.1:n.8370+123923C>T
NM_022336.4:c.1285G>A (EDAR) MANE Select	NP_071731.1:p.Ala429Thr