Canonical Allele Identifier: CA2579234693

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117172476A>G , CM000670.2:g.117172476A>G	GRCh38
NC_000008.10:g.118184715A>G , CM000670.1:g.118184715A>G	GRCh37
NC_000008.9:g.118253896A>G	NCBI36
NG_016991.1:g.227204A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.965-60A>G MANE Select	ENSP00000415011.2:n.965-60A>G
ENST00000427715.2:c.818-60A>G	ENSP00000407505.2:n.818-60A>G
ENST00000456015.6:c.965-60A>G	ENSP00000415011.2:n.965-60A>G
ENST00000519688.5:c.818-60A>G	ENSP00000431069.1:n.818-60A>G
ENST00000521243.5:c.818-60A>G	ENSP00000428545.1:n.818-60A>G
NM_001172811.1:c.818-60A>G	NP_001166282.1:n.818-60A>G
NM_001172813.1:c.818-60A>G	NP_001166284.1:n.818-60A>G
NM_001172814.1:c.818-60A>G	NP_001166285.1:n.818-60A>G
NM_001172815.1:c.818-60A>G	NP_001166286.1:n.818-60A>G
NM_173851.2:c.965-60A>G	NP_776250.2:n.965-60A>G
XM_011516881.1:c.965-60A>G	XP_011515183.1:n.965-60A>G
XM_011516882.1:c.818-60A>G	XP_011515184.1:n.818-60A>G
XR_928569.1:n.1020+139T>C
XR_928570.1:n.1020+139T>C
NM_001172815.2:c.818-60A>G	NP_001166286.1:n.818-60A>G
XM_024447083.1:c.818-60A>G	XP_024302851.1:n.818-60A>G
XR_928569.2:n.973+139T>C
XR_928570.2:n.973+139T>C
NM_001172811.2:c.818-60A>G	NP_001166282.1:n.818-60A>G
NM_001172813.2:c.818-60A>G	NP_001166284.1:n.818-60A>G
NM_001172814.2:c.818-60A>G	NP_001166285.1:n.818-60A>G
NM_173851.3:c.965-60A>G MANE Select	NP_776250.2:n.965-60A>G
NM_001172815.3:c.818-60A>G	NP_001166286.1:n.818-60A>G