Canonical Allele Identifier: CA653008281

Gene: SLC30A8

Linked Data

• COSMIC: COSN18733149

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117172758_117172759insC , CM000670.2:g.117172758_117172759insC	GRCh38
NC_000008.10:g.118184997_118184998insC , CM000670.1:g.118184997_118184998insC	GRCh37
NC_000008.9:g.118254178_118254179insC	NCBI36
NG_016991.1:g.227486_227487insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.*77_*78insC MANE Select	ENSP00000415011.2:n.*77_*78insC
ENST00000427715.2:c.*77_*78insC	ENSP00000407505.2:n.*77_*78insC
ENST00000456015.6:c.1187_1188insC	ENSP00000415011.2:n.1187_1188insC
ENST00000519688.5:c.*77_*78insC	ENSP00000431069.1:n.*77_*78insC
ENST00000521243.5:c.*77_*78insC	ENSP00000428545.1:n.*77_*78insC
NM_001172811.1:c.*77_*78insC	NP_001166282.1:n.*77_*78insC
NM_001172813.1:c.*77_*78insC	NP_001166284.1:n.*77_*78insC
NM_001172814.1:c.*77_*78insC	NP_001166285.1:n.*77_*78insC
NM_001172815.1:c.*77_*78insC	NP_001166286.1:n.*77_*78insC
NM_173851.2:c.*77_*78insC	NP_776250.2:n.*77_*78insC
XM_011516881.1:c.*77_*78insC	XP_011515183.1:n.*77_*78insC
XM_011516882.1:c.*77_*78insC	XP_011515184.1:n.*77_*78insC
XR_928569.1:n.890-14_890-13insG
XR_928570.1:n.890-14_890-13insG
NM_001172815.2:c.*77_*78insC	NP_001166286.1:n.*77_*78insC
XM_024447083.1:c.*77_*78insC	XP_024302851.1:n.*77_*78insC
XR_928569.2:n.843-14_843-13insG
XR_928570.2:n.843-14_843-13insG
NM_001172811.2:c.*77_*78insC	NP_001166282.1:n.*77_*78insC
NM_001172813.2:c.*77_*78insC	NP_001166284.1:n.*77_*78insC
NM_001172814.2:c.*77_*78insC	NP_001166285.1:n.*77_*78insC
NM_173851.3:c.*77_*78insC MANE Select	NP_776250.2:n.*77_*78insC
NM_001172815.3:c.*77_*78insC	NP_001166286.1:n.*77_*78insC