Canonical Allele Identifier: CA428087666

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109547432G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108930976G>C , CM000664.2:g.108930976G>C	GRCh38
NC_000002.11:g.109547432G>C , CM000664.1:g.109547432G>C	GRCh37
NC_000002.10:g.108913864G>C	NCBI36
NG_008257.1:g.63397C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.39C>G (EDAR) MANE Select	ENSP00000258443.2:p.Leu13=
ENST00000258443.6:c.39C>G (EDAR)	ENSP00000258443.2:p.Leu13=
ENST00000376651.1:c.39C>G (EDAR)	ENSP00000365839.1:p.Leu13=
ENST00000409271.5:c.39C>G (EDAR)	ENSP00000386371.1:p.Leu13=
NM_022336.3:c.39C>G (EDAR)	NP_071731.1:p.Leu13=
XM_006712204.1:c.39C>G (EDAR)	XP_006712267.1:p.Leu13=
XM_011510502.1:c.90C>G (EDAR)	XP_011508804.1:p.Leu30=
XM_011510503.1:c.90C>G (EDAR)	XP_011508805.1:p.Leu30=
XM_011510502.2:c.183C>G (EDAR)	XP_011508804.2:p.Leu61=
XM_011510503.2:c.183C>G (EDAR)	XP_011508805.2:p.Leu61=
XM_017004623.2:c.8370+157930G>C (RANBP2)	XP_016860112.1:n.8370+157930G>C
NM_022336.4:c.39C>G (EDAR) MANE Select	NP_071731.1:p.Leu13=