Canonical Allele Identifier: CA1732741585
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107683289_107683297delinsGTTAAGGAA , CM000669.2:g.107683289_107683297delinsGTTAAGGAA GRCh38
NC_000007.13:g.107323734_107323742delinsGTTAAGGAA , CM000669.1:g.107323734_107323742delinsGTTAAGGAA GRCh37
NC_000007.12:g.107110970_107110978delinsGTTAAGGAA NCBI36
NG_008489.1:g.27655_27663delinsGTTAAGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.853_861delinsGTTAAGGAA MANE Select ENSP00000494017.1:p.Val285=
ENST00000265715.7:c.853_861delinsGTTAAGGAA ENSP00000265715.3:p.Val285=
NM_000441.1:c.853_861delinsGTTAAGGAA NP_000432.1:p.Val285=
XM_005250425.1:c.853_861delinsGTTAAGGAA XP_005250482.1:p.Val285=
XM_006716025.2:c.853_861delinsGTTAAGGAA XP_006716088.1:p.Val285=
XM_005250425.2:c.853_861delinsGTTAAGGAA XP_005250482.1:p.Val285=
XM_006716025.3:c.853_861delinsGTTAAGGAA XP_006716088.1:p.Val285=
XM_017012318.1:c.853_861delinsGTTAAGGAA XP_016867807.1:p.Val285=
NM_000441.2:c.853_861delinsGTTAAGGAA MANE Select NP_000432.1:p.Val285=