Canonical Allele Identifier: CA1278354308

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897165_108897166delinsCG , CM000664.2:g.108897165_108897166delinsCG	GRCh38
NC_000002.11:g.109513621_109513622delinsCG , CM000664.1:g.109513621_109513622delinsCG	GRCh37
NC_000002.10:g.108880053_108880054delinsCG	NCBI36
NG_008257.1:g.97207_97208delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1088_1089delinsCG (EDAR) MANE Select	ENSP00000258443.2:p.Thr363=
ENST00000258443.6:c.1088_1089delinsCG (EDAR)	ENSP00000258443.2:p.Thr363=
ENST00000376651.1:c.1184_1185delinsCG (EDAR)	ENSP00000365839.1:p.Thr395=
ENST00000409271.5:c.1184_1185delinsCG (EDAR)	ENSP00000386371.1:p.Thr395=
NM_022336.3:c.1088_1089delinsCG (EDAR)	NP_071731.1:p.Thr363=
XM_006712204.1:c.1184_1185delinsCG (EDAR)	XP_006712267.1:p.Thr395=
XM_011510502.1:c.1235_1236delinsCG (EDAR)	XP_011508804.1:p.Thr412=
XM_011510503.1:c.1139_1140delinsCG (EDAR)	XP_011508805.1:p.Thr380=
XM_011510504.1:c.515_516delinsCG (EDAR)	XP_011508806.1:p.Thr172=
XM_011510502.2:c.1328_1329delinsCG (EDAR)	XP_011508804.2:p.Thr443=
XM_011510503.2:c.1232_1233delinsCG (EDAR)	XP_011508805.2:p.Thr411=
XM_017004623.2:c.8370+124119_8370+124120delinsCG (RANBP2)	XP_016860112.1:n.8370+124119_8370+124120delinsCG
NM_022336.4:c.1088_1089delinsCG (EDAR) MANE Select	NP_071731.1:p.Thr363=