Canonical Allele Identifier: CA10740839
Gene: SLAMF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160495121C>A , CM000663.2:g.160495121C>A GRCh38
NC_000001.10:g.160464911C>A , CM000663.1:g.160464911C>A GRCh37
NC_000001.9:g.158731535C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368057.8:c.382+940G>T MANE Select ENSP00000357036.3:n.382+940G>T
ENST00000368055.1:c.50-3733G>T ENSP00000357034.1:n.50-3733G>T
ENST00000368057.7:c.382+940G>T ENSP00000357036.3:n.382+940G>T
ENST00000368059.7:c.382+940G>T ENSP00000357038.3:n.382+940G>T
NM_001184714.1:c.382+940G>T NP_001171643.1:n.382+940G>T
NM_001184715.1:c.235+940G>T NP_001171644.1:n.235+940G>T
NM_001184716.1:c.50-3733G>T NP_001171645.1:n.50-3733G>T
NM_052931.4:c.382+940G>T NP_443163.1:n.382+940G>T
XM_017000215.2:c.382+940G>T XP_016855704.1:n.382+940G>T
XM_017000216.1:c.235+940G>T XP_016855705.1:n.235+940G>T
XM_017000217.1:c.50-3733G>T XP_016855706.1:n.50-3733G>T
NM_001184714.2:c.382+940G>T MANE Select NP_001171643.1:n.382+940G>T
NM_001184715.2:c.235+940G>T NP_001171644.1:n.235+940G>T
NM_001184716.2:c.50-3733G>T NP_001171645.1:n.50-3733G>T
NM_052931.5:c.382+940G>T NP_443163.1:n.382+940G>T