Canonical Allele Identifier: CA348047596

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513415A>C (hg19) ; chr2:g.108896959A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108896959A>C , CM000664.2:g.108896959A>C	GRCh38
NC_000002.11:g.109513415A>C , CM000664.1:g.109513415A>C	GRCh37
NC_000002.10:g.108879847A>C	NCBI36
NG_008257.1:g.97414T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.1295T>G (EDAR) MANE Select	ENSP00000258443.2:p.Leu432Arg
ENST00000258443.6:c.1295T>G (EDAR)	ENSP00000258443.2:p.Leu432Arg
ENST00000376651.1:c.1391T>G (EDAR)	ENSP00000365839.1:p.Leu464Arg
ENST00000409271.5:c.1391T>G (EDAR)	ENSP00000386371.1:p.Leu464Arg
NM_022336.3:c.1295T>G (EDAR)	NP_071731.1:p.Leu432Arg
XM_006712204.1:c.1391T>G (EDAR)	XP_006712267.1:p.Leu464Arg
XM_011510502.1:c.1442T>G (EDAR)	XP_011508804.1:p.Leu481Arg
XM_011510503.1:c.1346T>G (EDAR)	XP_011508805.1:p.Leu449Arg
XM_011510504.1:c.722T>G (EDAR)	XP_011508806.1:p.Leu241Arg
XM_011510502.2:c.1535T>G (EDAR)	XP_011508804.2:p.Leu512Arg
XM_011510503.2:c.1439T>G (EDAR)	XP_011508805.2:p.Leu480Arg
XM_017004623.2:c.8370+123913A>C (RANBP2)	XP_016860112.1:n.8370+123913A>C
NM_022336.4:c.1295T>G (EDAR) MANE Select	NP_071731.1:p.Leu432Arg