Canonical Allele Identifier: CA428203957

Gene: EDAR RANBP2

Linked Data

• MyVariant Identifiers: chr2:g.109513468T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897012T>C , CM000664.2:g.108897012T>C	GRCh38
NC_000002.11:g.109513468T>C , CM000664.1:g.109513468T>C	GRCh37
NC_000002.10:g.108879900T>C	NCBI36
NG_008257.1:g.97361A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.1242A>G (EDAR) MANE Select	ENSP00000258443.2:p.Lys414=
ENST00000258443.6:c.1242A>G (EDAR)	ENSP00000258443.2:p.Lys414=
ENST00000376651.1:c.1338A>G (EDAR)	ENSP00000365839.1:p.Lys446=
ENST00000409271.5:c.1338A>G (EDAR)	ENSP00000386371.1:p.Lys446=
NM_022336.3:c.1242A>G (EDAR)	NP_071731.1:p.Lys414=
XM_006712204.1:c.1338A>G (EDAR)	XP_006712267.1:p.Lys446=
XM_011510502.1:c.1389A>G (EDAR)	XP_011508804.1:p.Lys463=
XM_011510503.1:c.1293A>G (EDAR)	XP_011508805.1:p.Lys431=
XM_011510504.1:c.669A>G (EDAR)	XP_011508806.1:p.Lys223=
XM_011510502.2:c.1482A>G (EDAR)	XP_011508804.2:p.Lys494=
XM_011510503.2:c.1386A>G (EDAR)	XP_011508805.2:p.Lys462=
XM_017004623.2:c.8370+123966T>C (RANBP2)	XP_016860112.1:n.8370+123966T>C
NM_022336.4:c.1242A>G (EDAR) MANE Select	NP_071731.1:p.Lys414=