Canonical Allele Identifier: CA1278358772

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907578_108907579delinsGC , CM000664.2:g.108907578_108907579delinsGC	GRCh38
NC_000002.11:g.109524034_109524035delinsGC , CM000664.1:g.109524034_109524035delinsGC	GRCh37
NC_000002.10:g.108890466_108890467delinsGC	NCBI36
NG_008257.1:g.86794_86795delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.963+281_963+282delinsGC (EDAR) MANE Select	ENSP00000258443.2:n.963+281_963+282delinsGC
ENST00000258443.6:c.963+281_963+282delinsGC (EDAR)	ENSP00000258443.2:n.963+281_963+282delinsGC
ENST00000376651.1:c.1059+281_1059+282delinsGC (EDAR)	ENSP00000365839.1:n.1059+281_1059+282delinsGC
ENST00000409271.5:c.1059+281_1059+282delinsGC (EDAR)	ENSP00000386371.1:n.1059+281_1059+282delinsGC
NM_022336.3:c.963+281_963+282delinsGC (EDAR)	NP_071731.1:n.963+281_963+282delinsGC
XM_006712204.1:c.1059+281_1059+282delinsGC (EDAR)	XP_006712267.1:n.1059+281_1059+282delinsGC
XM_011510502.1:c.1110+281_1110+282delinsGC (EDAR)	XP_011508804.1:n.1110+281_1110+282delinsGC
XM_011510503.1:c.1014+281_1014+282delinsGC (EDAR)	XP_011508805.1:n.1014+281_1014+282delinsGC
XM_011510504.1:c.390+281_390+282delinsGC (EDAR)	XP_011508806.1:n.390+281_390+282delinsGC
XM_011510502.2:c.1203+281_1203+282delinsGC (EDAR)	XP_011508804.2:n.1203+281_1203+282delinsGC
XM_011510503.2:c.1107+281_1107+282delinsGC (EDAR)	XP_011508805.2:n.1107+281_1107+282delinsGC
XM_017004623.2:c.8370+134532_8370+134533delinsGC (RANBP2)	XP_016860112.1:n.8370+134532_8370+134533delinsGC
NM_022336.4:c.963+281_963+282delinsGC (EDAR) MANE Select	NP_071731.1:n.963+281_963+282delinsGC