Canonical Allele Identifier: CA348048134

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513569A>C (hg19) ; chr2:g.108897113A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897113A>C , CM000664.2:g.108897113A>C	GRCh38
NC_000002.11:g.109513569A>C , CM000664.1:g.109513569A>C	GRCh37
NC_000002.10:g.108880001A>C	NCBI36
NG_008257.1:g.97260T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.1141T>G (EDAR) MANE Select	ENSP00000258443.2:p.Phe381Val
ENST00000258443.6:c.1141T>G (EDAR)	ENSP00000258443.2:p.Phe381Val
ENST00000376651.1:c.1237T>G (EDAR)	ENSP00000365839.1:p.Phe413Val
ENST00000409271.5:c.1237T>G (EDAR)	ENSP00000386371.1:p.Phe413Val
NM_022336.3:c.1141T>G (EDAR)	NP_071731.1:p.Phe381Val
XM_006712204.1:c.1237T>G (EDAR)	XP_006712267.1:p.Phe413Val
XM_011510502.1:c.1288T>G (EDAR)	XP_011508804.1:p.Phe430Val
XM_011510503.1:c.1192T>G (EDAR)	XP_011508805.1:p.Phe398Val
XM_011510504.1:c.568T>G (EDAR)	XP_011508806.1:p.Phe190Val
XM_011510502.2:c.1381T>G (EDAR)	XP_011508804.2:p.Phe461Val
XM_011510503.2:c.1285T>G (EDAR)	XP_011508805.2:p.Phe429Val
XM_017004623.2:c.8370+124067A>C (RANBP2)	XP_016860112.1:n.8370+124067A>C
NM_022336.4:c.1141T>G (EDAR) MANE Select	NP_071731.1:p.Phe381Val