Canonical Allele Identifier: CA428203924

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513444A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108896988A>G , CM000664.2:g.108896988A>G	GRCh38
NC_000002.11:g.109513444A>G , CM000664.1:g.109513444A>G	GRCh37
NC_000002.10:g.108879876A>G	NCBI36
NG_008257.1:g.97385T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1266T>C (EDAR) MANE Select	ENSP00000258443.2:p.Asp422=
ENST00000258443.6:c.1266T>C (EDAR)	ENSP00000258443.2:p.Asp422=
ENST00000376651.1:c.1362T>C (EDAR)	ENSP00000365839.1:p.Asp454=
ENST00000409271.5:c.1362T>C (EDAR)	ENSP00000386371.1:p.Asp454=
NM_022336.3:c.1266T>C (EDAR)	NP_071731.1:p.Asp422=
XM_006712204.1:c.1362T>C (EDAR)	XP_006712267.1:p.Asp454=
XM_011510502.1:c.1413T>C (EDAR)	XP_011508804.1:p.Asp471=
XM_011510503.1:c.1317T>C (EDAR)	XP_011508805.1:p.Asp439=
XM_011510504.1:c.693T>C (EDAR)	XP_011508806.1:p.Asp231=
XM_011510502.2:c.1506T>C (EDAR)	XP_011508804.2:p.Asp502=
XM_011510503.2:c.1410T>C (EDAR)	XP_011508805.2:p.Asp470=
XM_017004623.2:c.8370+123942A>G (RANBP2)	XP_016860112.1:n.8370+123942A>G
NM_022336.4:c.1266T>C (EDAR) MANE Select	NP_071731.1:p.Asp422=