Canonical Allele Identifier: CA1930307585
Gene: SLIT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97148976C= , CM000672.2:g.97148976C= GRCh38
NC_000010.10:g.98908733C= , CM000672.1:g.98908733C= GRCh37
NC_000010.9:g.98898723C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266058.9:c.413+8842G= MANE Select ENSP00000266058.4:n.413+8842G=
ENST00000266058.8:c.413+8842G= ENSP00000266058.4:n.413+8842G=
ENST00000314867.9:c.362+8842G= ENSP00000315005.5:n.362+8842G=
ENST00000371041.3:c.413+8842G= ENSP00000360080.3:n.413+8842G=
ENST00000371070.8:c.413+8842G= ENSP00000360109.4:n.413+8842G=
NM_003061.2:c.413+8842G= NP_003052.2:n.413+8842G=
NM_003061.3:c.413+8842G= MANE Select NP_003052.2:n.413+8842G=