Canonical Allele Identifier: CA462465114

Gene: SLC30A8

Linked Data

• MyVariant Identifiers: chr8:g.118165325A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117153086A>C , CM000670.2:g.117153086A>C	GRCh38
NC_000008.10:g.118165325A>C , CM000670.1:g.118165325A>C	GRCh37
NC_000008.9:g.118234506A>C	NCBI36
NG_016991.1:g.207814A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.414A>C MANE Select	ENSP00000415011.2:p.Arg138=
ENST00000427715.2:c.267A>C	ENSP00000407505.2:p.Arg89=
ENST00000456015.6:c.414A>C	ENSP00000415011.2:p.Arg138=
ENST00000519688.5:c.267A>C	ENSP00000431069.1:p.Arg89=
ENST00000521243.5:c.267A>C	ENSP00000428545.1:p.Arg89=
NM_001172811.1:c.267A>C	NP_001166282.1:p.Arg89=
NM_001172813.1:c.267A>C	NP_001166284.1:p.Arg89=
NM_001172814.1:c.267A>C	NP_001166285.1:p.Arg89=
NM_001172815.1:c.267A>C	NP_001166286.1:p.Arg89=
NM_173851.2:c.414A>C	NP_776250.2:p.Arg138=
XM_011516881.1:c.414A>C	XP_011515183.1:p.Arg138=
XM_011516882.1:c.267A>C	XP_011515184.1:p.Arg89=
XR_928569.1:n.1020+19529T>G
XR_928570.1:n.1020+19529T>G
NM_001172815.2:c.267A>C	NP_001166286.1:p.Arg89=
XM_024447083.1:c.267A>C	XP_024302851.1:p.Arg89=
XR_928569.2:n.973+19529T>G
XR_928570.2:n.973+19529T>G
NM_001172811.2:c.267A>C	NP_001166282.1:p.Arg89=
NM_001172813.2:c.267A>C	NP_001166284.1:p.Arg89=
NM_001172814.2:c.267A>C	NP_001166285.1:p.Arg89=
NM_173851.3:c.414A>C MANE Select	NP_776250.2:p.Arg138=
NM_001172815.3:c.267A>C	NP_001166286.1:p.Arg89=