Canonical Allele Identifier: CA1278358643

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108907299_108907300delinsAC , CM000664.2:g.108907299_108907300delinsAC	GRCh38
NC_000002.11:g.109523755_109523756delinsAC , CM000664.1:g.109523755_109523756delinsAC	GRCh37
NC_000002.10:g.108890187_108890188delinsAC	NCBI36
NG_008257.1:g.87073_87074delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.963+560_963+561delinsGT (EDAR) MANE Select	ENSP00000258443.2:n.963+560_963+561delinsGT
ENST00000258443.6:c.963+560_963+561delinsGT (EDAR)	ENSP00000258443.2:n.963+560_963+561delinsGT
ENST00000376651.1:c.1059+560_1059+561delinsGT (EDAR)	ENSP00000365839.1:n.1059+560_1059+561delinsGT
ENST00000409271.5:c.1059+560_1059+561delinsGT (EDAR)	ENSP00000386371.1:n.1059+560_1059+561delinsGT
NM_022336.3:c.963+560_963+561delinsGT (EDAR)	NP_071731.1:n.963+560_963+561delinsGT
XM_006712204.1:c.1059+560_1059+561delinsGT (EDAR)	XP_006712267.1:n.1059+560_1059+561delinsGT
XM_011510502.1:c.1110+560_1110+561delinsGT (EDAR)	XP_011508804.1:n.1110+560_1110+561delinsGT
XM_011510503.1:c.1014+560_1014+561delinsGT (EDAR)	XP_011508805.1:n.1014+560_1014+561delinsGT
XM_011510504.1:c.390+560_390+561delinsGT (EDAR)	XP_011508806.1:n.390+560_390+561delinsGT
XM_011510502.2:c.1203+560_1203+561delinsGT (EDAR)	XP_011508804.2:n.1203+560_1203+561delinsGT
XM_011510503.2:c.1107+560_1107+561delinsGT (EDAR)	XP_011508805.2:n.1107+560_1107+561delinsGT
XM_017004623.2:c.8370+134253_8370+134254delinsAC (RANBP2)	XP_016860112.1:n.8370+134253_8370+134254delinsAC
NM_022336.4:c.963+560_963+561delinsGT (EDAR) MANE Select	NP_071731.1:n.963+560_963+561delinsGT