Canonical Allele Identifier: CA348047447

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513377G>C (hg19) ; chr2:g.108896921G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108896921G>C , CM000664.2:g.108896921G>C	GRCh38
NC_000002.11:g.109513377G>C , CM000664.1:g.109513377G>C	GRCh37
NC_000002.10:g.108879809G>C	NCBI36
NG_008257.1:g.97452C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1333C>G (EDAR) MANE Select	ENSP00000258443.2:p.His445Asp
ENST00000258443.6:c.1333C>G (EDAR)	ENSP00000258443.2:p.His445Asp
ENST00000376651.1:c.1429C>G (EDAR)	ENSP00000365839.1:p.His477Asp
ENST00000409271.5:c.1429C>G (EDAR)	ENSP00000386371.1:p.His477Asp
NM_022336.3:c.1333C>G (EDAR)	NP_071731.1:p.His445Asp
XM_006712204.1:c.1429C>G (EDAR)	XP_006712267.1:p.His477Asp
XM_011510502.1:c.1480C>G (EDAR)	XP_011508804.1:p.His494Asp
XM_011510503.1:c.1384C>G (EDAR)	XP_011508805.1:p.His462Asp
XM_011510504.1:c.760C>G (EDAR)	XP_011508806.1:p.His254Asp
XM_011510502.2:c.1573C>G (EDAR)	XP_011508804.2:p.His525Asp
XM_011510503.2:c.1477C>G (EDAR)	XP_011508805.2:p.His493Asp
XM_017004623.2:c.8370+123875G>C (RANBP2)	XP_016860112.1:n.8370+123875G>C
NM_022336.4:c.1333C>G (EDAR) MANE Select	NP_071731.1:p.His445Asp