Canonical Allele Identifier: CA1939105933
Gene: SLC18A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117262939_117262940delinsTA , CM000672.2:g.117262939_117262940delinsTA GRCh38
NC_000010.10:g.119022450_119022451delinsTA , CM000672.1:g.119022450_119022451delinsTA GRCh37
NC_000010.9:g.119012440_119012441delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000644641.2:c.992-3794_992-3793delinsTA MANE Select ENSP00000496339.1:n.992-3794_992-3793delinsTA
ENST00000298472.9:c.992-3794_992-3793delinsTA ENSP00000298472.5:n.992-3794_992-3793delinsTA
ENST00000497497.1:n.1408-3794_1408-3793delinsTA
NM_003054.4:c.992-3794_992-3793delinsTA NP_003045.2:n.992-3794_992-3793delinsTA
NM_003054.5:c.992-3794_992-3793delinsTA NP_003045.2:n.992-3794_992-3793delinsTA
NM_003054.6:c.992-3794_992-3793delinsTA MANE Select NP_003045.2:n.992-3794_992-3793delinsTA