Canonical Allele Identifier: CA348050982

Gene: EDAR RANBP2

Linked Data

• gnomAD v4: 2-108907933-G-T
• MyVariant Identifiers: chr2:g.109524389G>T (hg19) ; chr2:g.108907933G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907933G>T , CM000664.2:g.108907933G>T	GRCh38
NC_000002.11:g.109524389G>T , CM000664.1:g.109524389G>T	GRCh37
NC_000002.10:g.108890821G>T	NCBI36
NG_008257.1:g.86440C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.890C>A (EDAR) MANE Select	ENSP00000258443.2:p.Ser297Tyr
ENST00000258443.6:c.890C>A (EDAR)	ENSP00000258443.2:p.Ser297Tyr
ENST00000376651.1:c.986C>A (EDAR)	ENSP00000365839.1:p.Ser329Tyr
ENST00000409271.5:c.986C>A (EDAR)	ENSP00000386371.1:p.Ser329Tyr
NM_022336.3:c.890C>A (EDAR)	NP_071731.1:p.Ser297Tyr
XM_006712204.1:c.986C>A (EDAR)	XP_006712267.1:p.Ser329Tyr
XM_011510502.1:c.1037C>A (EDAR)	XP_011508804.1:p.Ser346Tyr
XM_011510503.1:c.941C>A (EDAR)	XP_011508805.1:p.Ser314Tyr
XM_011510504.1:c.317C>A (EDAR)	XP_011508806.1:p.Ser106Tyr
XM_011510502.2:c.1130C>A (EDAR)	XP_011508804.2:p.Ser377Tyr
XM_011510503.2:c.1034C>A (EDAR)	XP_011508805.2:p.Ser345Tyr
XM_017004623.2:c.8370+134887G>T (RANBP2)	XP_016860112.1:n.8370+134887G>T
NM_022336.4:c.890C>A (EDAR) MANE Select	NP_071731.1:p.Ser297Tyr