Canonical Allele Identifier: CA1813659788

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117173645_117173647delinsCTG , CM000670.2:g.117173645_117173647delinsCTG	GRCh38
NC_000008.10:g.118185884_118185886delinsCTG , CM000670.1:g.118185884_118185886delinsCTG	GRCh37
NC_000008.9:g.118255065_118255067delinsCTG	NCBI36
NG_016991.1:g.228373_228375delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.*964_*966delinsCTG MANE Select	ENSP00000415011.2:n.*964_*966delinsCTG
ENST00000427715.2:c.*964_*966delinsCTG	ENSP00000407505.2:n.*964_*966delinsCTG
ENST00000456015.6:c.2074_2076delinsCTG	ENSP00000415011.2:n.2074_2076delinsCTG
ENST00000519688.5:c.*964_*966delinsCTG	ENSP00000431069.1:n.*964_*966delinsCTG
NM_001172811.1:c.*964_*966delinsCTG	NP_001166282.1:n.*964_*966delinsCTG
NM_001172813.1:c.*964_*966delinsCTG	NP_001166284.1:n.*964_*966delinsCTG
NM_001172814.1:c.*964_*966delinsCTG	NP_001166285.1:n.*964_*966delinsCTG
NM_001172815.1:c.*964_*966delinsCTG	NP_001166286.1:n.*964_*966delinsCTG
NM_173851.2:c.*964_*966delinsCTG	NP_776250.2:n.*964_*966delinsCTG
XM_011516881.1:c.*964_*966delinsCTG	XP_011515183.1:n.*964_*966delinsCTG
XM_011516882.1:c.*964_*966delinsCTG	XP_011515184.1:n.*964_*966delinsCTG
XR_928566.1:n.920-159_920-157delinsCAG
XR_928567.1:n.513-159_513-157delinsCAG
XR_928568.1:n.718-159_718-157delinsCAG
XR_928569.1:n.761-159_761-157delinsCAG
XR_928570.1:n.761-159_761-157delinsCAG
NM_001172815.2:c.*964_*966delinsCTG	NP_001166286.1:n.*964_*966delinsCTG
XM_024447083.1:c.*964_*966delinsCTG	XP_024302851.1:n.*964_*966delinsCTG
XR_001746038.1:n.705-159_705-157delinsCAG
XR_928566.2:n.863-159_863-157delinsCAG
XR_928567.2:n.476-159_476-157delinsCAG
XR_928568.3:n.716-159_716-157delinsCAG
XR_928569.2:n.714-159_714-157delinsCAG
XR_928570.2:n.714-159_714-157delinsCAG
NM_001172811.2:c.*964_*966delinsCTG	NP_001166282.1:n.*964_*966delinsCTG
NM_001172813.2:c.*964_*966delinsCTG	NP_001166284.1:n.*964_*966delinsCTG
NM_001172814.2:c.*964_*966delinsCTG	NP_001166285.1:n.*964_*966delinsCTG
NM_173851.3:c.*964_*966delinsCTG MANE Select	NP_776250.2:n.*964_*966delinsCTG
NM_001172815.3:c.*964_*966delinsCTG	NP_001166286.1:n.*964_*966delinsCTG