Canonical Allele Identifier: CA348051095

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109524443A>C (hg19) ; chr2:g.108907987A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907987A>C , CM000664.2:g.108907987A>C	GRCh38
NC_000002.11:g.109524443A>C , CM000664.1:g.109524443A>C	GRCh37
NC_000002.10:g.108890875A>C	NCBI36
NG_008257.1:g.86386T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.836T>G (EDAR) MANE Select	ENSP00000258443.2:p.Leu279Arg
ENST00000258443.6:c.836T>G (EDAR)	ENSP00000258443.2:p.Leu279Arg
ENST00000376651.1:c.932T>G (EDAR)	ENSP00000365839.1:p.Leu311Arg
ENST00000409271.5:c.932T>G (EDAR)	ENSP00000386371.1:p.Leu311Arg
NM_022336.3:c.836T>G (EDAR)	NP_071731.1:p.Leu279Arg
XM_006712204.1:c.932T>G (EDAR)	XP_006712267.1:p.Leu311Arg
XM_011510502.1:c.983T>G (EDAR)	XP_011508804.1:p.Leu328Arg
XM_011510503.1:c.887T>G (EDAR)	XP_011508805.1:p.Leu296Arg
XM_011510504.1:c.263T>G (EDAR)	XP_011508806.1:p.Leu88Arg
XM_011510502.2:c.1076T>G (EDAR)	XP_011508804.2:p.Leu359Arg
XM_011510503.2:c.980T>G (EDAR)	XP_011508805.2:p.Leu327Arg
XM_017004623.2:c.8370+134941A>C (RANBP2)	XP_016860112.1:n.8370+134941A>C
NM_022336.4:c.836T>G (EDAR) MANE Select	NP_071731.1:p.Leu279Arg