Canonical Allele Identifier: CA462469041

Gene: SLC30A8

Linked Data

• MyVariant Identifiers: chr8:g.118184785G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117172546G>C , CM000670.2:g.117172546G>C	GRCh38
NC_000008.10:g.118184785G>C , CM000670.1:g.118184785G>C	GRCh37
NC_000008.9:g.118253966G>C	NCBI36
NG_016991.1:g.227274G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.975G>C MANE Select	ENSP00000415011.2:p.Arg325=
ENST00000427715.2:c.828G>C	ENSP00000407505.2:p.Arg276=
ENST00000456015.6:c.975G>C	ENSP00000415011.2:p.Arg325=
ENST00000519688.5:c.828G>C	ENSP00000431069.1:p.Arg276=
ENST00000521243.5:c.828G>C	ENSP00000428545.1:p.Arg276=
NM_001172811.1:c.828G>C	NP_001166282.1:p.Arg276=
NM_001172813.1:c.828G>C	NP_001166284.1:p.Arg276=
NM_001172814.1:c.828G>C	NP_001166285.1:p.Arg276=
NM_001172815.1:c.828G>C	NP_001166286.1:p.Arg276=
NM_173851.2:c.975G>C	NP_776250.2:p.Arg325=
XM_011516881.1:c.975G>C	XP_011515183.1:p.Arg325=
XM_011516882.1:c.828G>C	XP_011515184.1:p.Arg276=
XR_928569.1:n.1020+69C>G
XR_928570.1:n.1020+69C>G
NM_001172815.2:c.828G>C	NP_001166286.1:p.Arg276=
XM_024447083.1:c.828G>C	XP_024302851.1:p.Arg276=
XR_928569.2:n.973+69C>G
XR_928570.2:n.973+69C>G
NM_001172811.2:c.828G>C	NP_001166282.1:p.Arg276=
NM_001172813.2:c.828G>C	NP_001166284.1:p.Arg276=
NM_001172814.2:c.828G>C	NP_001166285.1:p.Arg276=
NM_173851.3:c.975G>C MANE Select	NP_776250.2:p.Arg325=
NM_001172815.3:c.828G>C	NP_001166286.1:p.Arg276=