Canonical Allele Identifier: CA348048196

Gene: EDAR RANBP2

Linked Data

• gnomAD v4: 2-108897142-A-C
• MyVariant Identifiers: chr2:g.109513598A>C (hg19) ; chr2:g.108897142A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897142A>C , CM000664.2:g.108897142A>C	GRCh38
NC_000002.11:g.109513598A>C , CM000664.1:g.109513598A>C	GRCh37
NC_000002.10:g.108880030A>C	NCBI36
NG_008257.1:g.97231T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.1112T>G (EDAR) MANE Select	ENSP00000258443.2:p.Val371Gly
ENST00000258443.6:c.1112T>G (EDAR)	ENSP00000258443.2:p.Val371Gly
ENST00000376651.1:c.1208T>G (EDAR)	ENSP00000365839.1:p.Val403Gly
ENST00000409271.5:c.1208T>G (EDAR)	ENSP00000386371.1:p.Val403Gly
NM_022336.3:c.1112T>G (EDAR)	NP_071731.1:p.Val371Gly
XM_006712204.1:c.1208T>G (EDAR)	XP_006712267.1:p.Val403Gly
XM_011510502.1:c.1259T>G (EDAR)	XP_011508804.1:p.Val420Gly
XM_011510503.1:c.1163T>G (EDAR)	XP_011508805.1:p.Val388Gly
XM_011510504.1:c.539T>G (EDAR)	XP_011508806.1:p.Val180Gly
XM_011510502.2:c.1352T>G (EDAR)	XP_011508804.2:p.Val451Gly
XM_011510503.2:c.1256T>G (EDAR)	XP_011508805.2:p.Val419Gly
XM_017004623.2:c.8370+124096A>C (RANBP2)	XP_016860112.1:n.8370+124096A>C
NM_022336.4:c.1112T>G (EDAR) MANE Select	NP_071731.1:p.Val371Gly