Canonical Allele Identifier: CA2684457467
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107661977_107661978insCACCAGAAGGGCGGCG , CM000669.2:g.107661977_107661978insCACCAGAAGGGCGGCG GRCh38
NC_000007.13:g.107302422_107302423insCACCAGAAGGGCGGCG , CM000669.1:g.107302422_107302423insCACCAGAAGGGCGGCG GRCh37
NC_000007.12:g.107089658_107089659insCACCAGAAGGGCGGCG NCBI36
NG_008489.1:g.6343_6344insCACCAGAAGGGCGGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.164+172_164+173insCACCAGAAGGGCGGCG MANE Select ENSP00000494017.1:n.164+172_164+173insCACCAGAAGGGCGGCG
ENST00000265715.7:c.164+172_164+173insCACCAGAAGGGCGGCG ENSP00000265715.3:n.164+172_164+173insCACCAGAAGGGCGGCG
ENST00000440056.1:c.164+172_164+173insCACCAGAAGGGCGGCG ENSP00000394760.1:n.164+172_164+173insCACCAGAAGGGCGGCG
NM_000441.1:c.164+172_164+173insCACCAGAAGGGCGGCG NP_000432.1:n.164+172_164+173insCACCAGAAGGGCGGCG
XM_005250425.1:c.164+172_164+173insCACCAGAAGGGCGGCG XP_005250482.1:n.164+172_164+173insCACCAGAAGGGCGGCG
XM_006716025.2:c.164+172_164+173insCACCAGAAGGGCGGCG XP_006716088.1:n.164+172_164+173insCACCAGAAGGGCGGCG
XM_005250425.2:c.164+172_164+173insCACCAGAAGGGCGGCG XP_005250482.1:n.164+172_164+173insCACCAGAAGGGCGGCG
XM_006716025.3:c.164+172_164+173insCACCAGAAGGGCGGCG XP_006716088.1:n.164+172_164+173insCACCAGAAGGGCGGCG
XM_017012318.1:c.164+172_164+173insCACCAGAAGGGCGGCG XP_016867807.1:n.164+172_164+173insCACCAGAAGGGCGGCG
NM_000441.2:c.164+172_164+173insCACCAGAAGGGCGGCG MANE Select NP_000432.1:n.164+172_164+173insCACCAGAAGGGCGGCG