Canonical Allele Identifier: CA2688340311

Gene: SLC30A8

Linked Data

• gnomAD v4: 8-117172810-C-CTATT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117172817_117172820dup , CM000670.2:g.117172817_117172820dup	GRCh38
NC_000008.10:g.118185056_118185059dup , CM000670.1:g.118185056_118185059dup	GRCh37
NC_000008.9:g.118254237_118254240dup	NCBI36
NG_016991.1:g.227545_227548dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.*136_*139dup MANE Select	ENSP00000415011.2:n.*136_*139dup
ENST00000427715.2:c.*136_*139dup	ENSP00000407505.2:n.*136_*139dup
ENST00000456015.6:c.1246_1249dup	ENSP00000415011.2:n.1246_1249dup
ENST00000519688.5:c.*136_*139dup	ENSP00000431069.1:n.*136_*139dup
NM_001172811.1:c.*136_*139dup	NP_001166282.1:n.*136_*139dup
NM_001172813.1:c.*136_*139dup	NP_001166284.1:n.*136_*139dup
NM_001172814.1:c.*136_*139dup	NP_001166285.1:n.*136_*139dup
NM_001172815.1:c.*136_*139dup	NP_001166286.1:n.*136_*139dup
NM_173851.2:c.*136_*139dup	NP_776250.2:n.*136_*139dup
XM_011516881.1:c.*136_*139dup	XP_011515183.1:n.*136_*139dup
XM_011516882.1:c.*136_*139dup	XP_011515184.1:n.*136_*139dup
XR_928569.1:n.890-69_890-66dup
XR_928570.1:n.890-69_890-66dup
NM_001172815.2:c.*136_*139dup	NP_001166286.1:n.*136_*139dup
XM_024447083.1:c.*136_*139dup	XP_024302851.1:n.*136_*139dup
XR_928569.2:n.843-69_843-66dup
XR_928570.2:n.843-69_843-66dup
NM_001172811.2:c.*136_*139dup	NP_001166282.1:n.*136_*139dup
NM_001172813.2:c.*136_*139dup	NP_001166284.1:n.*136_*139dup
NM_001172814.2:c.*136_*139dup	NP_001166285.1:n.*136_*139dup
NM_173851.3:c.*136_*139dup MANE Select	NP_776250.2:n.*136_*139dup
NM_001172815.3:c.*136_*139dup	NP_001166286.1:n.*136_*139dup