Canonical Allele Identifier: CA1813625379

Gene: SLC30A8

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.117142733_117142734delinsTC , CM000670.2:g.117142733_117142734delinsTC	GRCh38
NC_000008.10:g.118154972_118154973delinsTC , CM000670.1:g.118154972_118154973delinsTC	GRCh37
NC_000008.9:g.118224153_118224154delinsTC	NCBI36
NG_016991.1:g.197461_197462delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000456015.7:c.72-4221_72-4220delinsTC MANE Select	ENSP00000415011.2:n.72-4221_72-4220delinsTC
ENST00000427715.2:c.-106-4086_-106-4085delinsTC	ENSP00000407505.2:n.-106-4086_-106-4085delinsTC
ENST00000456015.6:c.72-4221_72-4220delinsTC	ENSP00000415011.2:n.72-4221_72-4220delinsTC
ENST00000518396.5:c.-106-4086_-106-4085delinsTC	ENSP00000485167.1:n.-106-4086_-106-4085delinsTC
ENST00000518521.5:c.-76-4221_-76-4220delinsTC	ENSP00000485566.1:n.-76-4221_-76-4220delinsTC
ENST00000519688.5:c.-106-4086_-106-4085delinsTC	ENSP00000431069.1:n.-106-4086_-106-4085delinsTC
ENST00000520469.1:n.326-4221_326-4220delinsTC
ENST00000521035.5:n.462-4086_462-4085delinsTC
ENST00000521243.5:c.-106-4086_-106-4085delinsTC	ENSP00000428545.1:n.-106-4086_-106-4085delinsTC
ENST00000524274.5:c.-106-4086_-106-4085delinsTC	ENSP00000427760.1:n.-106-4086_-106-4085delinsTC
NM_001172811.1:c.-106-4086_-106-4085delinsTC	NP_001166282.1:n.-106-4086_-106-4085delinsTC
NM_001172813.1:c.-106-4086_-106-4085delinsTC	NP_001166284.1:n.-106-4086_-106-4085delinsTC
NM_001172814.1:c.-106-4086_-106-4085delinsTC	NP_001166285.1:n.-106-4086_-106-4085delinsTC
NM_001172815.1:c.-106-4086_-106-4085delinsTC	NP_001166286.1:n.-106-4086_-106-4085delinsTC
NM_173851.2:c.72-4221_72-4220delinsTC	NP_776250.2:n.72-4221_72-4220delinsTC
XM_011516881.1:c.72-4221_72-4220delinsTC	XP_011515183.1:n.72-4221_72-4220delinsTC
XR_928569.1:n.1020+29881_1020+29882delinsGA
XR_928570.1:n.1021-24948_1021-24947delinsGA
NM_001172815.2:c.-106-4086_-106-4085delinsTC	NP_001166286.1:n.-106-4086_-106-4085delinsTC
XM_024447083.1:c.-106-4086_-106-4085delinsTC	XP_024302851.1:n.-106-4086_-106-4085delinsTC
XR_928569.2:n.973+29881_973+29882delinsGA
XR_928570.2:n.974-24948_974-24947delinsGA
NM_001172811.2:c.-106-4086_-106-4085delinsTC	NP_001166282.1:n.-106-4086_-106-4085delinsTC
NM_001172813.2:c.-106-4086_-106-4085delinsTC	NP_001166284.1:n.-106-4086_-106-4085delinsTC
NM_001172814.2:c.-106-4086_-106-4085delinsTC	NP_001166285.1:n.-106-4086_-106-4085delinsTC
NM_173851.3:c.72-4221_72-4220delinsTC MANE Select	NP_776250.2:n.72-4221_72-4220delinsTC
NM_001172815.3:c.-106-4086_-106-4085delinsTC	NP_001166286.1:n.-106-4086_-106-4085delinsTC