Canonical Allele Identifier: CA10844840
Gene: SLC30A7 HGNC NCBI
HNRNPA1P68 HGNC NCBI

Linked Data

dbSNP Id: rs11581062

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100941963A>G , CM000663.2:g.100941963A>G GRCh38
NC_000001.10:g.101407519A>G , CM000663.1:g.101407519A>G GRCh37
NC_000001.9:g.101180107A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357650.9:c.843-19865A>G (SLC30A7) MANE Select ENSP00000350278.4:n.843-19865A>G
ENST00000357650.8:c.843-19865A>G (SLC30A7) ENSP00000350278.4:n.843-19865A>G
ENST00000370112.8:c.843-19865A>G (SLC30A7) ENSP00000359130.4:n.843-19865A>G
ENST00000425806.2:n.33T>C (HNRNPA1P68)
NM_001144884.1:c.843-19865A>G (SLC30A7) NP_001138356.1:n.843-19865A>G
NM_133496.4:c.843-19865A>G (SLC30A7) NP_598003.2:n.843-19865A>G
XM_011540779.1:c.633-19865A>G (SLC30A7) XP_011539081.1:n.633-19865A>G
XR_246237.2:n.1028-19865A>G (SLC30A7)
XM_011540779.3:c.633-19865A>G (SLC30A7) XP_011539081.1:n.633-19865A>G
XM_017000400.2:c.843-19865A>G (SLC30A7) XP_016855889.1:n.843-19865A>G
XR_246237.3:n.1014-19865A>G (SLC30A7)
NM_133496.5:c.843-19865A>G (SLC30A7) MANE Select NP_598003.2:n.843-19865A>G
NM_001144884.2:c.843-19865A>G (SLC30A7) NP_001138356.1:n.843-19865A>G