Canonical Allele Identifier: CA371913051

Gene: SLC30A8

Linked Data

• MyVariant Identifiers: chr8:g.118184787A>C (hg19) ; chr8:g.117172548A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117172548A>C , CM000670.2:g.117172548A>C	GRCh38
NC_000008.10:g.118184787A>C , CM000670.1:g.118184787A>C	GRCh37
NC_000008.9:g.118253968A>C	NCBI36
NG_016991.1:g.227276A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456015.7:c.977A>C MANE Select	ENSP00000415011.2:p.Asp326Ala
ENST00000427715.2:c.830A>C	ENSP00000407505.2:p.Asp277Ala
ENST00000456015.6:c.977A>C	ENSP00000415011.2:p.Asp326Ala
ENST00000519688.5:c.830A>C	ENSP00000431069.1:p.Asp277Ala
ENST00000521243.5:c.830A>C	ENSP00000428545.1:p.Asp277Ala
NM_001172811.1:c.830A>C	NP_001166282.1:p.Asp277Ala
NM_001172813.1:c.830A>C	NP_001166284.1:p.Asp277Ala
NM_001172814.1:c.830A>C	NP_001166285.1:p.Asp277Ala
NM_001172815.1:c.830A>C	NP_001166286.1:p.Asp277Ala
NM_173851.2:c.977A>C	NP_776250.2:p.Asp326Ala
XM_011516881.1:c.977A>C	XP_011515183.1:p.Asp326Ala
XM_011516882.1:c.830A>C	XP_011515184.1:p.Asp277Ala
XR_928569.1:n.1020+67T>G
XR_928570.1:n.1020+67T>G
NM_001172815.2:c.830A>C	NP_001166286.1:p.Asp277Ala
XM_024447083.1:c.830A>C	XP_024302851.1:p.Asp277Ala
XR_928569.2:n.973+67T>G
XR_928570.2:n.973+67T>G
NM_001172811.2:c.830A>C	NP_001166282.1:p.Asp277Ala
NM_001172813.2:c.830A>C	NP_001166284.1:p.Asp277Ala
NM_001172814.2:c.830A>C	NP_001166285.1:p.Asp277Ala
NM_173851.3:c.977A>C MANE Select	NP_776250.2:p.Asp326Ala
NM_001172815.3:c.830A>C	NP_001166286.1:p.Asp277Ala