Canonical Allele Identifier: CA2781886769

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117153122G>C , CM000670.2:g.117153122G>C	GRCh38
NC_000008.10:g.118165361G>C , CM000670.1:g.118165361G>C	GRCh37
NC_000008.9:g.118234542G>C	NCBI36
NG_016991.1:g.207850G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.418+32G>C MANE Select	ENSP00000415011.2:n.418+32G>C
ENST00000427715.2:c.271+32G>C	ENSP00000407505.2:n.271+32G>C
ENST00000456015.6:c.418+32G>C	ENSP00000415011.2:n.418+32G>C
ENST00000519688.5:c.271+32G>C	ENSP00000431069.1:n.271+32G>C
ENST00000521243.5:c.271+32G>C	ENSP00000428545.1:n.271+32G>C
NM_001172811.1:c.271+32G>C	NP_001166282.1:n.271+32G>C
NM_001172813.1:c.271+32G>C	NP_001166284.1:n.271+32G>C
NM_001172814.1:c.271+32G>C	NP_001166285.1:n.271+32G>C
NM_001172815.1:c.271+32G>C	NP_001166286.1:n.271+32G>C
NM_173851.2:c.418+32G>C	NP_776250.2:n.418+32G>C
XM_011516881.1:c.418+32G>C	XP_011515183.1:n.418+32G>C
XM_011516882.1:c.271+32G>C	XP_011515184.1:n.271+32G>C
XR_928569.1:n.1020+19493C>G
XR_928570.1:n.1020+19493C>G
NM_001172815.2:c.271+32G>C	NP_001166286.1:n.271+32G>C
XM_024447083.1:c.271+32G>C	XP_024302851.1:n.271+32G>C
XR_928569.2:n.973+19493C>G
XR_928570.2:n.973+19493C>G
NM_001172811.2:c.271+32G>C	NP_001166282.1:n.271+32G>C
NM_001172813.2:c.271+32G>C	NP_001166284.1:n.271+32G>C
NM_001172814.2:c.271+32G>C	NP_001166285.1:n.271+32G>C
NM_173851.3:c.418+32G>C MANE Select	NP_776250.2:n.418+32G>C
NM_001172815.3:c.271+32G>C	NP_001166286.1:n.271+32G>C