Canonical Allele Identifier: CA164215112
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1048600047

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107695839_107695842del , CM000669.2:g.107695839_107695842del GRCh38
NC_000007.13:g.107336284_107336287del , CM000669.1:g.107336284_107336287del GRCh37
NC_000007.12:g.107123520_107123523del NCBI36
NG_008489.1:g.40205_40208del

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1438-94_1438-91del MANE Select ENSP00000494017.1:n.1438-94_1438-91del
ENST00000644846.1:c.149-94_149-91del
ENST00000265715.7:c.1438-94_1438-91del ENSP00000265715.3:n.1438-94_1438-91del
ENST00000460748.1:n.541-94_541-91del
ENST00000477350.5:n.285-94_285-91del
ENST00000480841.5:n.287-94_287-91del
ENST00000497446.5:n.453-94_453-91del
NM_000441.1:c.1438-94_1438-91del NP_000432.1:n.1438-94_1438-91del
XM_005250425.1:c.1438-94_1438-91del XP_005250482.1:n.1438-94_1438-91del
XM_005250425.2:c.1438-94_1438-91del XP_005250482.1:n.1438-94_1438-91del
XM_017012318.1:c.1360-94_1360-91del XP_016867807.1:n.1360-94_1360-91del
NM_000441.2:c.1438-94_1438-91del MANE Select NP_000432.1:n.1438-94_1438-91del