Canonical Allele Identifier: CA13249884
Gene: SLIT1 HGNC NCBI
COSMIC:
COSN17458436 (not active)
MyVariant.info:
GRCh38 chr10:g.97049946A>G
GRCh37 chr10:g.98809703A>G
gnomAD v2:
10:98809703 A / G
gnomAD v3:
10:97049946 A / G
gnomAD v4:
chr10-97049946-A-G
Joint Max Group AF 0.32318343 (AFR)
Genomes Max Group AF 0.32318343 (AFR)
dbSNP:
7902871
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.97049946A>G , CM000672.2:g.97049946A>G GRCh38
NC_000010.10:g.98809703A>G , CM000672.1:g.98809703A>G GRCh37
NC_000010.9:g.98799693A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266058.9:c.1302-828T>C MANE Select ENSP00000266058.4:n.1302-828T>C
ENST00000266058.8:c.1302-828T>C ENSP00000266058.4:n.1302-828T>C
ENST00000314867.9:c.1281-828T>C ENSP00000315005.5:n.1281-828T>C
ENST00000371070.8:c.1302-828T>C ENSP00000360109.4:n.1302-828T>C
NM_003061.2:c.1302-828T>C NP_003052.2:n.1302-828T>C
NM_003061.3:c.1302-828T>C MANE Select NP_003052.2:n.1302-828T>C
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