Canonical Allele Identifier: CA348047908

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513487A>G (hg19) ; chr2:g.108897031A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897031A>G , CM000664.2:g.108897031A>G	GRCh38
NC_000002.11:g.109513487A>G , CM000664.1:g.109513487A>G	GRCh37
NC_000002.10:g.108879919A>G	NCBI36
NG_008257.1:g.97342T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1223T>C (EDAR) MANE Select	ENSP00000258443.2:p.Ile408Thr
ENST00000258443.6:c.1223T>C (EDAR)	ENSP00000258443.2:p.Ile408Thr
ENST00000376651.1:c.1319T>C (EDAR)	ENSP00000365839.1:p.Ile440Thr
ENST00000409271.5:c.1319T>C (EDAR)	ENSP00000386371.1:p.Ile440Thr
NM_022336.3:c.1223T>C (EDAR)	NP_071731.1:p.Ile408Thr
XM_006712204.1:c.1319T>C (EDAR)	XP_006712267.1:p.Ile440Thr
XM_011510502.1:c.1370T>C (EDAR)	XP_011508804.1:p.Ile457Thr
XM_011510503.1:c.1274T>C (EDAR)	XP_011508805.1:p.Ile425Thr
XM_011510504.1:c.650T>C (EDAR)	XP_011508806.1:p.Ile217Thr
XM_011510502.2:c.1463T>C (EDAR)	XP_011508804.2:p.Ile488Thr
XM_011510503.2:c.1367T>C (EDAR)	XP_011508805.2:p.Ile456Thr
XM_017004623.2:c.8370+123985A>G (RANBP2)	XP_016860112.1:n.8370+123985A>G
NM_022336.4:c.1223T>C (EDAR) MANE Select	NP_071731.1:p.Ile408Thr