Canonical Allele Identifier: CA427910878

Gene: EDAR RANBP2

Linked Data

• gnomAD v4: 2-108897195-G-T
• MyVariant Identifiers: chr2:g.109513651G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897195G>T , CM000664.2:g.108897195G>T	GRCh38
NC_000002.11:g.109513651G>T , CM000664.1:g.109513651G>T	GRCh37
NC_000002.10:g.108880083G>T	NCBI36
NG_008257.1:g.97178C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1059C>A (EDAR) MANE Select	ENSP00000258443.2:p.Leu353=
ENST00000258443.6:c.1059C>A (EDAR)	ENSP00000258443.2:p.Leu353=
ENST00000376651.1:c.1155C>A (EDAR)	ENSP00000365839.1:p.Leu385=
ENST00000409271.5:c.1155C>A (EDAR)	ENSP00000386371.1:p.Leu385=
NM_022336.3:c.1059C>A (EDAR)	NP_071731.1:p.Leu353=
XM_006712204.1:c.1155C>A (EDAR)	XP_006712267.1:p.Leu385=
XM_011510502.1:c.1206C>A (EDAR)	XP_011508804.1:p.Leu402=
XM_011510503.1:c.1110C>A (EDAR)	XP_011508805.1:p.Leu370=
XM_011510504.1:c.486C>A (EDAR)	XP_011508806.1:p.Leu162=
XM_011510502.2:c.1299C>A (EDAR)	XP_011508804.2:p.Leu433=
XM_011510503.2:c.1203C>A (EDAR)	XP_011508805.2:p.Leu401=
XM_017004623.2:c.8370+124149G>T (RANBP2)	XP_016860112.1:n.8370+124149G>T
NM_022336.4:c.1059C>A (EDAR) MANE Select	NP_071731.1:p.Leu353=