Canonical Allele Identifier: CA2660592781

Gene: EDAR RANBP2

Linked Data

• gnomAD v4: 2-108908055-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108908061_108908062dup , CM000664.2:g.108908061_108908062dup	GRCh38
NC_000002.11:g.109524517_109524518dup , CM000664.1:g.109524517_109524518dup	GRCh37
NC_000002.10:g.108890949_108890950dup	NCBI36
NG_008257.1:g.86316_86317dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.804-38_804-37dup (EDAR) MANE Select	ENSP00000258443.2:n.804-38_804-37dup
ENST00000258443.6:c.804-38_804-37dup (EDAR)	ENSP00000258443.2:n.804-38_804-37dup
ENST00000376651.1:c.900-38_900-37dup (EDAR)	ENSP00000365839.1:n.900-38_900-37dup
ENST00000409271.5:c.900-38_900-37dup (EDAR)	ENSP00000386371.1:n.900-38_900-37dup
NM_022336.3:c.804-38_804-37dup (EDAR)	NP_071731.1:n.804-38_804-37dup
XM_006712204.1:c.900-38_900-37dup (EDAR)	XP_006712267.1:n.900-38_900-37dup
XM_011510502.1:c.951-38_951-37dup (EDAR)	XP_011508804.1:n.951-38_951-37dup
XM_011510503.1:c.855-38_855-37dup (EDAR)	XP_011508805.1:n.855-38_855-37dup
XM_011510504.1:c.231-38_231-37dup (EDAR)	XP_011508806.1:n.231-38_231-37dup
XM_011510502.2:c.1044-38_1044-37dup (EDAR)	XP_011508804.2:n.1044-38_1044-37dup
XM_011510503.2:c.948-38_948-37dup (EDAR)	XP_011508805.2:n.948-38_948-37dup
XM_017004623.2:c.8370+135015_8370+135016dup (RANBP2)	XP_016860112.1:n.8370+135015_8370+135016dup
NM_022336.4:c.804-38_804-37dup (EDAR) MANE Select	NP_071731.1:n.804-38_804-37dup