Canonical Allele Identifier: CA1278354428

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108897418_108897420delinsAAG , CM000664.2:g.108897418_108897420delinsAAG	GRCh38
NC_000002.11:g.109513874_109513876delinsAAG , CM000664.1:g.109513874_109513876delinsAAG	GRCh37
NC_000002.10:g.108880306_108880308delinsAAG	NCBI36
NG_008257.1:g.96953_96955delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258443.7:c.1025-191_1025-189delinsCTT (EDAR) MANE Select	ENSP00000258443.2:n.1025-191_1025-189delinsCTT
ENST00000258443.6:c.1025-191_1025-189delinsCTT (EDAR)	ENSP00000258443.2:n.1025-191_1025-189delinsCTT
ENST00000376651.1:c.1121-191_1121-189delinsCTT (EDAR)	ENSP00000365839.1:n.1121-191_1121-189delinsCTT
ENST00000409271.5:c.1121-191_1121-189delinsCTT (EDAR)	ENSP00000386371.1:n.1121-191_1121-189delinsCTT
NM_022336.3:c.1025-191_1025-189delinsCTT (EDAR)	NP_071731.1:n.1025-191_1025-189delinsCTT
XM_006712204.1:c.1121-191_1121-189delinsCTT (EDAR)	XP_006712267.1:n.1121-191_1121-189delinsCTT
XM_011510502.1:c.1172-191_1172-189delinsCTT (EDAR)	XP_011508804.1:n.1172-191_1172-189delinsCTT
XM_011510503.1:c.1076-191_1076-189delinsCTT (EDAR)	XP_011508805.1:n.1076-191_1076-189delinsCTT
XM_011510504.1:c.452-191_452-189delinsCTT (EDAR)	XP_011508806.1:n.452-191_452-189delinsCTT
XM_011510502.2:c.1265-191_1265-189delinsCTT (EDAR)	XP_011508804.2:n.1265-191_1265-189delinsCTT
XM_011510503.2:c.1169-191_1169-189delinsCTT (EDAR)	XP_011508805.2:n.1169-191_1169-189delinsCTT
XM_017004623.2:c.8370+124372_8370+124374delinsAAG (RANBP2)	XP_016860112.1:n.8370+124372_8370+124374delinsAAG
NM_022336.4:c.1025-191_1025-189delinsCTT (EDAR) MANE Select	NP_071731.1:n.1025-191_1025-189delinsCTT