Canonical Allele Identifier: CA1881104970

Gene: NCS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130205003G= , CM000671.2:g.130205003G=	GRCh38
NC_000009.11:g.132967282G= , CM000671.1:g.132967282G=	GRCh37
NC_000009.10:g.132007103G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372398.6:c.89+4021G= MANE Select	ENSP00000361475.3:n.89+4021G=
ENST00000372398.5:c.89+4021G=	ENSP00000361475.3:n.89+4021G=
ENST00000493042.1:n.143+4021G=
ENST00000630865.1:c.35+4021G=	ENSP00000486695.1:n.35+4021G=
NM_001128826.1:c.35+4021G=	NP_001122298.1:n.35+4021G=
NM_014286.3:c.89+4021G=	NP_055101.2:n.89+4021G=
NM_014286.4:c.89+4021G= MANE Select	NP_055101.2:n.89+4021G=
NM_001128826.2:c.35+4021G=	NP_001122298.1:n.35+4021G=