Canonical Allele Identifier: CA2224361181
Gene: SLC12A3 HGNC NCBI

Linked Data

dbSNP Id: rs2055434771

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56894482_56894483del , CM000678.2:g.56894482_56894483del GRCh38
NC_000016.9:g.56928394_56928395del , CM000678.1:g.56928394_56928395del GRCh37
NC_000016.8:g.55485895_55485896del NCBI36
NG_009386.1:g.34276_34277del
NG_009386.2:g.34276_34277del

Transcript Alleles

HGVS Amino-acid change
ENST00000563236.6:c.2522-49_2522-48del MANE Select ENSP00000456149.2:n.2522-49_2522-48del
ENST00000262502.5:c.2519-49_2519-48del ENSP00000262502.5:n.2519-49_2519-48del
ENST00000438926.6:c.2549-49_2549-48del ENSP00000402152.2:n.2549-49_2549-48del
ENST00000563236.5:c.2522-49_2522-48del ENSP00000456149.1:n.2522-49_2522-48del
ENST00000566786.5:c.2546-49_2546-48del ENSP00000457552.1:n.2546-49_2546-48del
NM_000339.2:c.2549-49_2549-48del NP_000330.2:n.2549-49_2549-48del
NM_001126107.1:c.2546-49_2546-48del NP_001119579.1:n.2546-49_2546-48del
NM_001126108.1:c.2522-49_2522-48del NP_001119580.1:n.2522-49_2522-48del
XM_005256119.1:c.2519-49_2519-48del XP_005256176.1:n.2519-49_2519-48del
XM_005256119.2:c.2519-49_2519-48del XP_005256176.1:n.2519-49_2519-48del
NM_000339.3:c.2549-49_2549-48del NP_000330.3:n.2549-49_2549-48del
NM_001126107.2:c.2546-49_2546-48del NP_001119579.2:n.2546-49_2546-48del
NM_001126108.2:c.2522-49_2522-48del MANE Select NP_001119580.2:n.2522-49_2522-48del