Canonical Allele Identifier: CA1139861234

Gene: SLAMF6

Genomic Alleles

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

Transcript Alleles

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