Canonical Allele Identifier: CA419203529

Gene: SLC30A7

Linked Data

• MyVariant Identifiers: chr1:g.101377784T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100912228T>C , CM000663.2:g.100912228T>C	GRCh38
NC_000001.10:g.101377784T>C , CM000663.1:g.101377784T>C	GRCh37
NC_000001.9:g.101150372T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357650.9:c.501T>C MANE Select	ENSP00000350278.4:p.Ser167=
ENST00000357650.8:c.501T>C	ENSP00000350278.4:p.Ser167=
ENST00000370112.8:c.501T>C	ENSP00000359130.4:p.Ser167=
NM_001144884.1:c.501T>C	NP_001138356.1:p.Ser167=
NM_133496.4:c.501T>C	NP_598003.2:p.Ser167=
XM_011540779.1:c.291T>C	XP_011539081.1:p.Ser97=
XR_246237.2:n.686T>C
XM_011540779.3:c.291T>C	XP_011539081.1:p.Ser97=
XM_017000400.2:c.501T>C	XP_016855889.1:p.Ser167=
XM_017000401.2:c.501T>C	XP_016855890.1:p.Ser167=
XR_246237.3:n.672T>C
NM_133496.5:c.501T>C MANE Select	NP_598003.2:p.Ser167=
NM_001144884.2:c.501T>C	NP_001138356.1:p.Ser167=