Canonical Allele Identifier: CA427911934

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109524388G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907932G>T , CM000664.2:g.108907932G>T	GRCh38
NC_000002.11:g.109524388G>T , CM000664.1:g.109524388G>T	GRCh37
NC_000002.10:g.108890820G>T	NCBI36
NG_008257.1:g.86441C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.891C>A (EDAR) MANE Select	ENSP00000258443.2:p.Ser297=
ENST00000258443.6:c.891C>A (EDAR)	ENSP00000258443.2:p.Ser297=
ENST00000376651.1:c.987C>A (EDAR)	ENSP00000365839.1:p.Ser329=
ENST00000409271.5:c.987C>A (EDAR)	ENSP00000386371.1:p.Ser329=
NM_022336.3:c.891C>A (EDAR)	NP_071731.1:p.Ser297=
XM_006712204.1:c.987C>A (EDAR)	XP_006712267.1:p.Ser329=
XM_011510502.1:c.1038C>A (EDAR)	XP_011508804.1:p.Ser346=
XM_011510503.1:c.942C>A (EDAR)	XP_011508805.1:p.Ser314=
XM_011510504.1:c.318C>A (EDAR)	XP_011508806.1:p.Ser106=
XM_011510502.2:c.1131C>A (EDAR)	XP_011508804.2:p.Ser377=
XM_011510503.2:c.1035C>A (EDAR)	XP_011508805.2:p.Ser345=
XM_017004623.2:c.8370+134886G>T (RANBP2)	XP_016860112.1:n.8370+134886G>T
NM_022336.4:c.891C>A (EDAR) MANE Select	NP_071731.1:p.Ser297=