Canonical Allele Identifier: CA584429215

Gene: SLC30A8

Linked Data

• dbSNP Id: rs1235668999
• gnomAD v2: 8-118185819-T-C
• gnomAD v3: 8-117173580-T-C
• gnomAD v4: 8-117173580-T-C
• MyVariant Identifiers: chr8:g.118185819T>C (hg19) ; chr8:g.117173580T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117173580T>C , CM000670.2:g.117173580T>C	GRCh38
NC_000008.10:g.118185819T>C , CM000670.1:g.118185819T>C	GRCh37
NC_000008.9:g.118255000T>C	NCBI36
NG_016991.1:g.228308T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.*899T>C MANE Select	ENSP00000415011.2:n.*899T>C
ENST00000427715.2:c.*899T>C	ENSP00000407505.2:n.*899T>C
ENST00000456015.6:c.2009T>C	ENSP00000415011.2:n.2009T>C
ENST00000519688.5:c.*899T>C	ENSP00000431069.1:n.*899T>C
NM_001172811.1:c.*899T>C	NP_001166282.1:n.*899T>C
NM_001172813.1:c.*899T>C	NP_001166284.1:n.*899T>C
NM_001172814.1:c.*899T>C	NP_001166285.1:n.*899T>C
NM_001172815.1:c.*899T>C	NP_001166286.1:n.*899T>C
NM_173851.2:c.*899T>C	NP_776250.2:n.*899T>C
XM_011516881.1:c.*899T>C	XP_011515183.1:n.*899T>C
XM_011516882.1:c.*899T>C	XP_011515184.1:n.*899T>C
XR_928566.1:n.920-92A>G
XR_928567.1:n.513-92A>G
XR_928568.1:n.718-92A>G
XR_928569.1:n.761-92A>G
XR_928570.1:n.761-92A>G
NM_001172815.2:c.*899T>C	NP_001166286.1:n.*899T>C
XM_024447083.1:c.*899T>C	XP_024302851.1:n.*899T>C
XR_001746038.1:n.705-92A>G
XR_928566.2:n.863-92A>G
XR_928567.2:n.476-92A>G
XR_928568.3:n.716-92A>G
XR_928569.2:n.714-92A>G
XR_928570.2:n.714-92A>G
NM_001172811.2:c.*899T>C	NP_001166282.1:n.*899T>C
NM_001172813.2:c.*899T>C	NP_001166284.1:n.*899T>C
NM_001172814.2:c.*899T>C	NP_001166285.1:n.*899T>C
NM_173851.3:c.*899T>C MANE Select	NP_776250.2:n.*899T>C
NM_001172815.3:c.*899T>C	NP_001166286.1:n.*899T>C