Canonical Allele Identifier: CA428086827

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109545707C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108929251C>T , CM000664.2:g.108929251C>T	GRCh38
NC_000002.11:g.109545707C>T , CM000664.1:g.109545707C>T	GRCh37
NC_000002.10:g.108912139C>T	NCBI36
NG_008257.1:g.65122G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.303G>A (EDAR) MANE Select	ENSP00000258443.2:p.Val101=
ENST00000258443.6:c.303G>A (EDAR)	ENSP00000258443.2:p.Val101=
ENST00000376651.1:c.303G>A (EDAR)	ENSP00000365839.1:p.Val101=
ENST00000409271.5:c.303G>A (EDAR)	ENSP00000386371.1:p.Val101=
NM_022336.3:c.303G>A (EDAR)	NP_071731.1:p.Val101=
XM_006712204.1:c.303G>A (EDAR)	XP_006712267.1:p.Val101=
XM_011510502.1:c.354G>A (EDAR)	XP_011508804.1:p.Val118=
XM_011510503.1:c.354G>A (EDAR)	XP_011508805.1:p.Val118=
XM_011510502.2:c.447G>A (EDAR)	XP_011508804.2:p.Val149=
XM_011510503.2:c.447G>A (EDAR)	XP_011508805.2:p.Val149=
XM_017004623.2:c.8370+156205C>T (RANBP2)	XP_016860112.1:n.8370+156205C>T
NM_022336.4:c.303G>A (EDAR) MANE Select	NP_071731.1:p.Val101=