Canonical Allele Identifier: CA1939105958
Gene: SLC18A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117263021_117263023delinsCTG , CM000672.2:g.117263021_117263023delinsCTG GRCh38
NC_000010.10:g.119022532_119022534delinsCTG , CM000672.1:g.119022532_119022534delinsCTG GRCh37
NC_000010.9:g.119012522_119012524delinsCTG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000644641.2:c.992-3712_992-3710delinsCTG MANE Select ENSP00000496339.1:n.992-3712_992-3710deli...
ENST00000298472.9:c.992-3712_992-3710delinsCTG ENSP00000298472.5:n.992-3712_992-3710deli...
ENST00000497497.1:n.1408-3712_1408-3710delinsCTG
NM_003054.4:c.992-3712_992-3710delinsCTG NP_003045.2:n.992-3712_992-3710delinsCTG
NM_003054.5:c.992-3712_992-3710delinsCTG NP_003045.2:n.992-3712_992-3710delinsCTG
NM_003054.6:c.992-3712_992-3710delinsCTG MANE Select NP_003045.2:n.992-3712_992-3710delinsCTG