Canonical Allele Identifier: CA622338970
Gene: SLC12A3 HGNC NCBI

Linked Data

dbSNP Id: rs1212100867

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56887798_56887802del , CM000678.2:g.56887798_56887802del GRCh38
NC_000016.9:g.56921710_56921714del , CM000678.1:g.56921710_56921714del GRCh37
NC_000016.8:g.55479211_55479215del NCBI36
NG_009386.1:g.27592_27596del
NG_009386.2:g.27592_27596del

Transcript Alleles

HGVS Amino-acid Change
ENST00000563236.6:c.2179-127_2179-123del MANE Select ENSP00000456149.2:n.2179-127_2179-123del
ENST00000262502.5:c.2176-127_2176-123del ENSP00000262502.5:n.2176-127_2176-123del
ENST00000438926.6:c.2179-127_2179-123del ENSP00000402152.2:n.2179-127_2179-123del
ENST00000563236.5:c.2179-127_2179-123del ENSP00000456149.1:n.2179-127_2179-123del
ENST00000566786.5:c.2176-127_2176-123del ENSP00000457552.1:n.2176-127_2176-123del
NM_000339.2:c.2179-127_2179-123del NP_000330.2:n.2179-127_2179-123del
NM_001126107.1:c.2176-127_2176-123del NP_001119579.1:n.2176-127_2176-123del
NM_001126108.1:c.2179-127_2179-123del NP_001119580.1:n.2179-127_2179-123del
XM_005256119.1:c.2176-127_2176-123del XP_005256176.1:n.2176-127_2176-123del
XM_005256119.2:c.2176-127_2176-123del XP_005256176.1:n.2176-127_2176-123del
NM_000339.3:c.2179-127_2179-123del NP_000330.3:n.2179-127_2179-123del
NM_001126107.2:c.2176-127_2176-123del NP_001119579.2:n.2176-127_2176-123del
NM_001126108.2:c.2179-127_2179-123del MANE Select NP_001119580.2:n.2179-127_2179-123del