Canonical Allele Identifier: CA348051050

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109524420C>A (hg19) ; chr2:g.108907964C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907964C>A , CM000664.2:g.108907964C>A	GRCh38
NC_000002.11:g.109524420C>A , CM000664.1:g.109524420C>A	GRCh37
NC_000002.10:g.108890852C>A	NCBI36
NG_008257.1:g.86409G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.859G>T (EDAR) MANE Select	ENSP00000258443.2:p.Asp287Tyr
ENST00000258443.6:c.859G>T (EDAR)	ENSP00000258443.2:p.Asp287Tyr
ENST00000376651.1:c.955G>T (EDAR)	ENSP00000365839.1:p.Asp319Tyr
ENST00000409271.5:c.955G>T (EDAR)	ENSP00000386371.1:p.Asp319Tyr
NM_022336.3:c.859G>T (EDAR)	NP_071731.1:p.Asp287Tyr
XM_006712204.1:c.955G>T (EDAR)	XP_006712267.1:p.Asp319Tyr
XM_011510502.1:c.1006G>T (EDAR)	XP_011508804.1:p.Asp336Tyr
XM_011510503.1:c.910G>T (EDAR)	XP_011508805.1:p.Asp304Tyr
XM_011510504.1:c.286G>T (EDAR)	XP_011508806.1:p.Asp96Tyr
XM_011510502.2:c.1099G>T (EDAR)	XP_011508804.2:p.Asp367Tyr
XM_011510503.2:c.1003G>T (EDAR)	XP_011508805.2:p.Asp335Tyr
XM_017004623.2:c.8370+134918C>A (RANBP2)	XP_016860112.1:n.8370+134918C>A
NM_022336.4:c.859G>T (EDAR) MANE Select	NP_071731.1:p.Asp287Tyr