Canonical Allele Identifier: CA2633373011
Gene: SLC12A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56883928_56883931del , CM000678.2:g.56883928_56883931del GRCh38
NC_000016.9:g.56917840_56917843del , CM000678.1:g.56917840_56917843del GRCh37
NC_000016.8:g.55475341_55475344del NCBI36
NG_009386.1:g.23722_23725del
NG_009386.2:g.23722_23725del

Transcript Alleles

HGVS Amino-acid Change
ENST00000563236.6:c.1670-121_1670-118del MANE Select ENSP00000456149.2:n.1670-121_1670-118del
ENST00000262502.5:c.1667-121_1667-118del ENSP00000262502.5:n.1667-121_1667-118del
ENST00000438926.6:c.1670-121_1670-118del ENSP00000402152.2:n.1670-121_1670-118del
ENST00000563236.5:c.1670-121_1670-118del ENSP00000456149.1:n.1670-121_1670-118del
ENST00000566786.5:c.1667-121_1667-118del ENSP00000457552.1:n.1667-121_1667-118del
NM_000339.2:c.1670-121_1670-118del NP_000330.2:n.1670-121_1670-118del
NM_001126107.1:c.1667-121_1667-118del NP_001119579.1:n.1667-121_1667-118del
NM_001126108.1:c.1670-121_1670-118del NP_001119580.1:n.1670-121_1670-118del
XM_005256119.1:c.1667-121_1667-118del XP_005256176.1:n.1667-121_1667-118del
XM_005256119.2:c.1667-121_1667-118del XP_005256176.1:n.1667-121_1667-118del
NM_000339.3:c.1670-121_1670-118del NP_000330.3:n.1670-121_1670-118del
NM_001126107.2:c.1667-121_1667-118del NP_001119579.2:n.1667-121_1667-118del
NM_001126108.2:c.1670-121_1670-118del MANE Select NP_001119580.2:n.1670-121_1670-118del