Canonical Allele Identifier: CA2586969752

Gene: EDAR RANBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.108929278_108929279insGCG , CM000664.2:g.108929278_108929279insGCG	GRCh38
NC_000002.11:g.109545734_109545735insGCG , CM000664.1:g.109545734_109545735insGCG	GRCh37
NC_000002.10:g.108912166_108912167insGCG	NCBI36
NG_008257.1:g.65095_65096insGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000258443.7:c.276_277insGCC (EDAR) MANE Select	ENSP00000258443.2:p.Asp92_Cys93insAla
ENST00000258443.6:c.276_277insGCC (EDAR)	ENSP00000258443.2:p.Asp92_Cys93insAla
ENST00000376651.1:c.276_277insGCC (EDAR)	ENSP00000365839.1:p.Asp92_Cys93insAla
ENST00000409271.5:c.276_277insGCC (EDAR)	ENSP00000386371.1:p.Asp92_Cys93insAla
NM_022336.3:c.276_277insGCC (EDAR)	NP_071731.1:p.Asp92_Cys93insAla
XM_006712204.1:c.276_277insGCC (EDAR)	XP_006712267.1:p.Asp92_Cys93insAla
XM_011510502.1:c.327_328insGCC (EDAR)	XP_011508804.1:p.Asp109_Cys110insAla
XM_011510503.1:c.327_328insGCC (EDAR)	XP_011508805.1:p.Asp109_Cys110insAla
XM_011510502.2:c.420_421insGCC (EDAR)	XP_011508804.2:p.Asp140_Cys141insAla
XM_011510503.2:c.420_421insGCC (EDAR)	XP_011508805.2:p.Asp140_Cys141insAla
XM_017004623.2:c.8370+156232_8370+156233insGCG (RANBP2)	XP_016860112.1:n.8370+156232_8370+156233i...
NM_022336.4:c.276_277insGCC (EDAR) MANE Select	NP_071731.1:p.Asp92_Cys93insAla