Canonical Allele Identifier: CA348047400

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513364C>A (hg19) ; chr2:g.108896908C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108896908C>A , CM000664.2:g.108896908C>A	GRCh38
NC_000002.11:g.109513364C>A , CM000664.1:g.109513364C>A	GRCh37
NC_000002.10:g.108879796C>A	NCBI36
NG_008257.1:g.97465G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.1346G>T (EDAR) MANE Select	ENSP00000258443.2:p.Ter449Leu
ENST00000258443.6:c.1346G>T (EDAR)	ENSP00000258443.2:p.Ter449Leu
ENST00000376651.1:c.1442G>T (EDAR)	ENSP00000365839.1:p.Ter481Leu
ENST00000409271.5:c.1442G>T (EDAR)	ENSP00000386371.1:p.Ter481Leu
NM_022336.3:c.1346G>T (EDAR)	NP_071731.1:p.Ter449Leu
XM_006712204.1:c.1442G>T (EDAR)	XP_006712267.1:p.Ter481Leu
XM_011510502.1:c.1493G>T (EDAR)	XP_011508804.1:p.Ter498Leu
XM_011510503.1:c.1397G>T (EDAR)	XP_011508805.1:p.Ter466Leu
XM_011510504.1:c.773G>T (EDAR)	XP_011508806.1:p.Ter258Leu
XM_011510502.2:c.1586G>T (EDAR)	XP_011508804.2:p.Ter529Leu
XM_011510503.2:c.1490G>T (EDAR)	XP_011508805.2:p.Ter497Leu
XM_017004623.2:c.8370+123862C>A (RANBP2)	XP_016860112.1:n.8370+123862C>A
NM_022336.4:c.1346G>T (EDAR) MANE Select	NP_071731.1:p.Ter449Leu