Canonical Allele Identifier: CA1184348151

Gene: SLC30A7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100912120A= , CM000663.2:g.100912120A=	GRCh38
NC_000001.10:g.101377676A= , CM000663.1:g.101377676A=	GRCh37
NC_000001.9:g.101150264A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357650.9:c.393A= MANE Select	ENSP00000350278.4:p.Leu131=
ENST00000357650.8:c.393A=	ENSP00000350278.4:p.Leu131=
ENST00000370112.8:c.393A=	ENSP00000359130.4:p.Leu131=
NM_001144884.1:c.393A=	NP_001138356.1:p.Leu131=
NM_133496.4:c.393A=	NP_598003.2:p.Leu131=
XM_011540779.1:c.183A=	XP_011539081.1:p.Leu61=
XR_246237.2:n.578A=
XM_011540779.3:c.183A=	XP_011539081.1:p.Leu61=
XM_017000400.2:c.393A=	XP_016855889.1:p.Leu131=
XM_017000401.2:c.393A=	XP_016855890.1:p.Leu131=
XR_246237.3:n.564A=
NM_133496.5:c.393A= MANE Select	NP_598003.2:p.Leu131=
NM_001144884.2:c.393A=	NP_001138356.1:p.Leu131=