Canonical Allele Identifier: CA27534004

Gene: SLC30A7 HNRNPA1P68

Linked Data

• dbSNP Id: rs1039793716
• gnomAD v3: 1-100941905-C-G
• gnomAD v4: 1-100941905-C-G
• MyVariant Identifiers: chr1:g.101407461C>G (hg19) ; chr1:g.100941905C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100941905C>G , CM000663.2:g.100941905C>G	GRCh38
NC_000001.10:g.101407461C>G , CM000663.1:g.101407461C>G	GRCh37
NC_000001.9:g.101180049C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357650.9:c.843-19923C>G (SLC30A7) MANE Select	ENSP00000350278.4:n.843-19923C>G
ENST00000357650.8:c.843-19923C>G (SLC30A7)	ENSP00000350278.4:n.843-19923C>G
ENST00000370112.8:c.843-19923C>G (SLC30A7)	ENSP00000359130.4:n.843-19923C>G
ENST00000425806.2:n.91G>C (HNRNPA1P68)
NM_001144884.1:c.843-19923C>G (SLC30A7)	NP_001138356.1:n.843-19923C>G
NM_133496.4:c.843-19923C>G (SLC30A7)	NP_598003.2:n.843-19923C>G
XM_011540779.1:c.633-19923C>G (SLC30A7)	XP_011539081.1:n.633-19923C>G
XR_246237.2:n.1028-19923C>G (SLC30A7)
XM_011540779.3:c.633-19923C>G (SLC30A7)	XP_011539081.1:n.633-19923C>G
XM_017000400.2:c.843-19923C>G (SLC30A7)	XP_016855889.1:n.843-19923C>G
XR_246237.3:n.1014-19923C>G (SLC30A7)
NM_133496.5:c.843-19923C>G (SLC30A7) MANE Select	NP_598003.2:n.843-19923C>G
NM_001144884.2:c.843-19923C>G (SLC30A7)	NP_001138356.1:n.843-19923C>G