Canonical Allele Identifier: CA2558861294

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108929418A>T , CM000664.2:g.108929418A>T	GRCh38
NC_000002.11:g.109545874A>T , CM000664.1:g.109545874A>T	GRCh37
NC_000002.10:g.108912306A>T	NCBI36
NG_008257.1:g.64955T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.175-39T>A (EDAR) MANE Select	ENSP00000258443.2:n.175-39T>A
ENST00000258443.6:c.175-39T>A (EDAR)	ENSP00000258443.2:n.175-39T>A
ENST00000376651.1:c.175-39T>A (EDAR)	ENSP00000365839.1:n.175-39T>A
ENST00000409271.5:c.175-39T>A (EDAR)	ENSP00000386371.1:n.175-39T>A
NM_022336.3:c.175-39T>A (EDAR)	NP_071731.1:n.175-39T>A
XM_006712204.1:c.175-39T>A (EDAR)	XP_006712267.1:n.175-39T>A
XM_011510502.1:c.226-39T>A (EDAR)	XP_011508804.1:n.226-39T>A
XM_011510503.1:c.226-39T>A (EDAR)	XP_011508805.1:n.226-39T>A
XM_011510502.2:c.319-39T>A (EDAR)	XP_011508804.2:n.319-39T>A
XM_011510503.2:c.319-39T>A (EDAR)	XP_011508805.2:n.319-39T>A
XM_017004623.2:c.8370+156372A>T (RANBP2)	XP_016860112.1:n.8370+156372A>T
NM_022336.4:c.175-39T>A (EDAR) MANE Select	NP_071731.1:n.175-39T>A