Canonical Allele Identifier: CA348051150

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109524466A>C (hg19) ; chr2:g.108908010A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108908010A>C , CM000664.2:g.108908010A>C	GRCh38
NC_000002.11:g.109524466A>C , CM000664.1:g.109524466A>C	GRCh37
NC_000002.10:g.108890898A>C	NCBI36
NG_008257.1:g.86363T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.813T>G (EDAR) MANE Select	ENSP00000258443.2:p.Asp271Glu
ENST00000258443.6:c.813T>G (EDAR)	ENSP00000258443.2:p.Asp271Glu
ENST00000376651.1:c.909T>G (EDAR)	ENSP00000365839.1:p.Asp303Glu
ENST00000409271.5:c.909T>G (EDAR)	ENSP00000386371.1:p.Asp303Glu
NM_022336.3:c.813T>G (EDAR)	NP_071731.1:p.Asp271Glu
XM_006712204.1:c.909T>G (EDAR)	XP_006712267.1:p.Asp303Glu
XM_011510502.1:c.960T>G (EDAR)	XP_011508804.1:p.Asp320Glu
XM_011510503.1:c.864T>G (EDAR)	XP_011508805.1:p.Asp288Glu
XM_011510504.1:c.240T>G (EDAR)	XP_011508806.1:p.Asp80Glu
XM_011510502.2:c.1053T>G (EDAR)	XP_011508804.2:p.Asp351Glu
XM_011510503.2:c.957T>G (EDAR)	XP_011508805.2:p.Asp319Glu
XM_017004623.2:c.8370+134964A>C (RANBP2)	XP_016860112.1:n.8370+134964A>C
NM_022336.4:c.813T>G (EDAR) MANE Select	NP_071731.1:p.Asp271Glu