Canonical Allele Identifier: CA1278358730

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907488_108907491delinsTATA , CM000664.2:g.108907488_108907491delinsTATA	GRCh38
NC_000002.11:g.109523944_109523947delinsTATA , CM000664.1:g.109523944_109523947delinsTATA	GRCh37
NC_000002.10:g.108890376_108890379delinsTATA	NCBI36
NG_008257.1:g.86882_86885delinsTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.963+369_963+372delinsTATA (EDAR) MANE Select	ENSP00000258443.2:n.963+369_963+372delinsTATA
ENST00000258443.6:c.963+369_963+372delinsTATA (EDAR)	ENSP00000258443.2:n.963+369_963+372delinsTATA
ENST00000376651.1:c.1059+369_1059+372delinsTATA (EDAR)	ENSP00000365839.1:n.1059+369_1059+372delinsTATA
ENST00000409271.5:c.1059+369_1059+372delinsTATA (EDAR)	ENSP00000386371.1:n.1059+369_1059+372delinsTATA
NM_022336.3:c.963+369_963+372delinsTATA (EDAR)	NP_071731.1:n.963+369_963+372delinsTATA
XM_006712204.1:c.1059+369_1059+372delinsTATA (EDAR)	XP_006712267.1:n.1059+369_1059+372delinsTATA
XM_011510502.1:c.1110+369_1110+372delinsTATA (EDAR)	XP_011508804.1:n.1110+369_1110+372delinsTATA
XM_011510503.1:c.1014+369_1014+372delinsTATA (EDAR)	XP_011508805.1:n.1014+369_1014+372delinsTATA
XM_011510504.1:c.390+369_390+372delinsTATA (EDAR)	XP_011508806.1:n.390+369_390+372delinsTATA
XM_011510502.2:c.1203+369_1203+372delinsTATA (EDAR)	XP_011508804.2:n.1203+369_1203+372delinsTATA
XM_011510503.2:c.1107+369_1107+372delinsTATA (EDAR)	XP_011508805.2:n.1107+369_1107+372delinsTATA
XM_017004623.2:c.8370+134442_8370+134445delinsTATA (RANBP2)	XP_016860112.1:n.8370+134442_8370+134445delinsTATA
NM_022336.4:c.963+369_963+372delinsTATA (EDAR) MANE Select	NP_071731.1:n.963+369_963+372delinsTATA