Canonical Allele Identifier: CA2578988614
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107675104_107675105dup , CM000669.2:g.107675104_107675105dup GRCh38
NC_000007.13:g.107315549_107315550dup , CM000669.1:g.107315549_107315550dup GRCh37
NC_000007.12:g.107102785_107102786dup NCBI36
NG_008489.1:g.19470_19471dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.760_761dup MANE Select ENSP00000494017.1:p.Tyr255SerfsTer?
ENST00000265715.7:c.760_761dup ENSP00000265715.3:p.Tyr255SerfsTer?
NM_000441.1:c.760_761dup NP_000432.1:p.Tyr255SerfsTer?
XM_005250425.1:c.760_761dup XP_005250482.1:p.Tyr255SerfsTer?
XM_006716025.2:c.760_761dup XP_006716088.1:p.Tyr255SerfsTer?
XM_005250425.2:c.760_761dup XP_005250482.1:p.Tyr255SerfsTer?
XM_006716025.3:c.760_761dup XP_006716088.1:p.Tyr255SerfsTer?
XM_017012318.1:c.760_761dup XP_016867807.1:p.Tyr255SerfsTer?
NM_000441.2:c.760_761dup MANE Select NP_000432.1:p.Tyr255SerfsTer?