Canonical Allele Identifier: CA2700108589

Gene: EDAR RANBP2

Linked Data

• dbSNP Id: rs1315725030

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907305_108907307del , CM000664.2:g.108907305_108907307del	GRCh38
NC_000002.11:g.109523761_109523763del , CM000664.1:g.109523761_109523763del	GRCh37
NC_000002.10:g.108890193_108890195del	NCBI36
NG_008257.1:g.87069_87071del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.963+556_963+558del (EDAR) MANE Select	ENSP00000258443.2:n.963+556_963+558del
ENST00000258443.6:c.963+556_963+558del (EDAR)	ENSP00000258443.2:n.963+556_963+558del
ENST00000376651.1:c.1059+556_1059+558del (EDAR)	ENSP00000365839.1:n.1059+556_1059+558del
ENST00000409271.5:c.1059+556_1059+558del (EDAR)	ENSP00000386371.1:n.1059+556_1059+558del
NM_022336.3:c.963+556_963+558del (EDAR)	NP_071731.1:n.963+556_963+558del
XM_006712204.1:c.1059+556_1059+558del (EDAR)	XP_006712267.1:n.1059+556_1059+558del
XM_011510502.1:c.1110+556_1110+558del (EDAR)	XP_011508804.1:n.1110+556_1110+558del
XM_011510503.1:c.1014+556_1014+558del (EDAR)	XP_011508805.1:n.1014+556_1014+558del
XM_011510504.1:c.390+556_390+558del (EDAR)	XP_011508806.1:n.390+556_390+558del
XM_011510502.2:c.1203+556_1203+558del (EDAR)	XP_011508804.2:n.1203+556_1203+558del
XM_011510503.2:c.1107+556_1107+558del (EDAR)	XP_011508805.2:n.1107+556_1107+558del
XM_017004623.2:c.8370+134259_8370+134261del (RANBP2)	XP_016860112.1:n.8370+134259_8370+134261del
NM_022336.4:c.963+556_963+558del (EDAR) MANE Select	NP_071731.1:n.963+556_963+558del