Canonical Allele Identifier: CA2581734417

Gene: SLAMF6

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160500468C>G , CM000663.2:g.160500468C>G	GRCh38
NC_000001.10:g.160470258C>G , CM000663.1:g.160470258C>G	GRCh37
NC_000001.9:g.158736882C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368057.8:c.50-4075G>C MANE Select	ENSP00000357036.3:n.50-4075G>C
ENST00000368055.1:c.50-9080G>C	ENSP00000357034.1:n.50-9080G>C
ENST00000368057.7:c.50-4075G>C	ENSP00000357036.3:n.50-4075G>C
ENST00000368059.7:c.50-4075G>C	ENSP00000357038.3:n.50-4075G>C
NM_001184714.1:c.50-4075G>C	NP_001171643.1:n.50-4075G>C
NM_001184715.1:c.50-4222G>C	NP_001171644.1:n.50-4222G>C
NM_001184716.1:c.50-9080G>C	NP_001171645.1:n.50-9080G>C
NM_052931.4:c.50-4075G>C	NP_443163.1:n.50-4075G>C
XM_017000215.2:c.50-4075G>C	XP_016855704.1:n.50-4075G>C
XM_017000216.1:c.50-4222G>C	XP_016855705.1:n.50-4222G>C
XM_017000217.1:c.50-9080G>C	XP_016855706.1:n.50-9080G>C
NM_001184714.2:c.50-4075G>C MANE Select	NP_001171643.1:n.50-4075G>C
NM_001184715.2:c.50-4222G>C	NP_001171644.1:n.50-4222G>C
NM_001184716.2:c.50-9080G>C	NP_001171645.1:n.50-9080G>C
NM_052931.5:c.50-4075G>C	NP_443163.1:n.50-4075G>C