Canonical Allele Identifier: CA419202880

Gene: SLC30A7

Linked Data

• MyVariant Identifiers: chr1:g.101377682T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100912126T>G , CM000663.2:g.100912126T>G	GRCh38
NC_000001.10:g.101377682T>G , CM000663.1:g.101377682T>G	GRCh37
NC_000001.9:g.101150270T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357650.9:c.399T>G MANE Select	ENSP00000350278.4:p.Pro133=
ENST00000357650.8:c.399T>G	ENSP00000350278.4:p.Pro133=
ENST00000370112.8:c.399T>G	ENSP00000359130.4:p.Pro133=
NM_001144884.1:c.399T>G	NP_001138356.1:p.Pro133=
NM_133496.4:c.399T>G	NP_598003.2:p.Pro133=
XM_011540779.1:c.189T>G	XP_011539081.1:p.Pro63=
XR_246237.2:n.584T>G
XM_011540779.3:c.189T>G	XP_011539081.1:p.Pro63=
XM_017000400.2:c.399T>G	XP_016855889.1:p.Pro133=
XM_017000401.2:c.399T>G	XP_016855890.1:p.Pro133=
XR_246237.3:n.570T>G
NM_133496.5:c.399T>G MANE Select	NP_598003.2:p.Pro133=
NM_001144884.2:c.399T>G	NP_001138356.1:p.Pro133=