Canonical Allele Identifier: CA1939105931

Gene: SLC18A2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117262934_117262935delinsCT , CM000672.2:g.117262934_117262935delinsCT	GRCh38
NC_000010.10:g.119022445_119022446delinsCT , CM000672.1:g.119022445_119022446delinsCT	GRCh37
NC_000010.9:g.119012435_119012436delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000644641.2:c.992-3799_992-3798delinsCT MANE Select	ENSP00000496339.1:n.992-3799_992-3798delinsCT
ENST00000298472.9:c.992-3799_992-3798delinsCT	ENSP00000298472.5:n.992-3799_992-3798delinsCT
ENST00000497497.1:n.1408-3799_1408-3798delinsCT
NM_003054.4:c.992-3799_992-3798delinsCT	NP_003045.2:n.992-3799_992-3798delinsCT
NM_003054.5:c.992-3799_992-3798delinsCT	NP_003045.2:n.992-3799_992-3798delinsCT
NM_003054.6:c.992-3799_992-3798delinsCT MANE Select	NP_003045.2:n.992-3799_992-3798delinsCT