Canonical Allele Identifier: CA200465912
Gene: NCS1 HGNC NCBI

Linked Data

dbSNP Id: rs545777034

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130204975G>A , CM000671.2:g.130204975G>A GRCh38
NC_000009.11:g.132967254G>A , CM000671.1:g.132967254G>A GRCh37
NC_000009.10:g.132007075G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000372398.6:c.89+3993G>A MANE Select ENSP00000361475.3:n.89+3993G>A
ENST00000372398.5:c.89+3993G>A ENSP00000361475.3:n.89+3993G>A
ENST00000493042.1:n.143+3993G>A
ENST00000630865.1:c.35+3993G>A ENSP00000486695.1:n.35+3993G>A
NM_001128826.1:c.35+3993G>A NP_001122298.1:n.35+3993G>A
NM_014286.3:c.89+3993G>A NP_055101.2:n.89+3993G>A
NM_014286.4:c.89+3993G>A MANE Select NP_055101.2:n.89+3993G>A
NM_001128826.2:c.35+3993G>A NP_001122298.1:n.35+3993G>A