Canonical Allele Identifier: CA1881104852

Gene: NCS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130204908_130204910delinsCTT , CM000671.2:g.130204908_130204910delinsCTT	GRCh38
NC_000009.11:g.132967187_132967189delinsCTT , CM000671.1:g.132967187_132967189delinsCTT	GRCh37
NC_000009.10:g.132007008_132007010delinsCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372398.6:c.89+3926_89+3928delinsCTT MANE Select	ENSP00000361475.3:n.89+3926_89+3928delinsCTT
ENST00000372398.5:c.89+3926_89+3928delinsCTT	ENSP00000361475.3:n.89+3926_89+3928delinsCTT
ENST00000493042.1:n.143+3926_143+3928delinsCTT
ENST00000630865.1:c.35+3926_35+3928delinsCTT	ENSP00000486695.1:n.35+3926_35+3928delinsCTT
NM_001128826.1:c.35+3926_35+3928delinsCTT	NP_001122298.1:n.35+3926_35+3928delinsCTT
NM_014286.3:c.89+3926_89+3928delinsCTT	NP_055101.2:n.89+3926_89+3928delinsCTT
NM_014286.4:c.89+3926_89+3928delinsCTT MANE Select	NP_055101.2:n.89+3926_89+3928delinsCTT
NM_001128826.2:c.35+3926_35+3928delinsCTT	NP_001122298.1:n.35+3926_35+3928delinsCTT