Canonical Allele Identifier: CA428203902

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513423T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108896967T>G , CM000664.2:g.108896967T>G	GRCh38
NC_000002.11:g.109513423T>G , CM000664.1:g.109513423T>G	GRCh37
NC_000002.10:g.108879855T>G	NCBI36
NG_008257.1:g.97406A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1287A>C (EDAR) MANE Select	ENSP00000258443.2:p.Ala429=
ENST00000258443.6:c.1287A>C (EDAR)	ENSP00000258443.2:p.Ala429=
ENST00000376651.1:c.1383A>C (EDAR)	ENSP00000365839.1:p.Ala461=
ENST00000409271.5:c.1383A>C (EDAR)	ENSP00000386371.1:p.Ala461=
NM_022336.3:c.1287A>C (EDAR)	NP_071731.1:p.Ala429=
XM_006712204.1:c.1383A>C (EDAR)	XP_006712267.1:p.Ala461=
XM_011510502.1:c.1434A>C (EDAR)	XP_011508804.1:p.Ala478=
XM_011510503.1:c.1338A>C (EDAR)	XP_011508805.1:p.Ala446=
XM_011510504.1:c.714A>C (EDAR)	XP_011508806.1:p.Ala238=
XM_011510502.2:c.1527A>C (EDAR)	XP_011508804.2:p.Ala509=
XM_011510503.2:c.1431A>C (EDAR)	XP_011508805.2:p.Ala477=
XM_017004623.2:c.8370+123921T>G (RANBP2)	XP_016860112.1:n.8370+123921T>G
NM_022336.4:c.1287A>C (EDAR) MANE Select	NP_071731.1:p.Ala429=