Canonical Allele Identifier: CA1278358810

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907647_108907648delinsTC , CM000664.2:g.108907647_108907648delinsTC	GRCh38
NC_000002.11:g.109524103_109524104delinsTC , CM000664.1:g.109524103_109524104delinsTC	GRCh37
NC_000002.10:g.108890535_108890536delinsTC	NCBI36
NG_008257.1:g.86725_86726delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.963+212_963+213delinsGA (EDAR) MANE Select	ENSP00000258443.2:n.963+212_963+213delinsGA
ENST00000258443.6:c.963+212_963+213delinsGA (EDAR)	ENSP00000258443.2:n.963+212_963+213delinsGA
ENST00000376651.1:c.1059+212_1059+213delinsGA (EDAR)	ENSP00000365839.1:n.1059+212_1059+213delinsGA
ENST00000409271.5:c.1059+212_1059+213delinsGA (EDAR)	ENSP00000386371.1:n.1059+212_1059+213delinsGA
NM_022336.3:c.963+212_963+213delinsGA (EDAR)	NP_071731.1:n.963+212_963+213delinsGA
XM_006712204.1:c.1059+212_1059+213delinsGA (EDAR)	XP_006712267.1:n.1059+212_1059+213delinsGA
XM_011510502.1:c.1110+212_1110+213delinsGA (EDAR)	XP_011508804.1:n.1110+212_1110+213delinsGA
XM_011510503.1:c.1014+212_1014+213delinsGA (EDAR)	XP_011508805.1:n.1014+212_1014+213delinsGA
XM_011510504.1:c.390+212_390+213delinsGA (EDAR)	XP_011508806.1:n.390+212_390+213delinsGA
XM_011510502.2:c.1203+212_1203+213delinsGA (EDAR)	XP_011508804.2:n.1203+212_1203+213delinsGA
XM_011510503.2:c.1107+212_1107+213delinsGA (EDAR)	XP_011508805.2:n.1107+212_1107+213delinsGA
XM_017004623.2:c.8370+134601_8370+134602delinsTC (RANBP2)	XP_016860112.1:n.8370+134601_8370+134602delinsTC
NM_022336.4:c.963+212_963+213delinsGA (EDAR) MANE Select	NP_071731.1:n.963+212_963+213delinsGA