Canonical Allele Identifier: CA651810801
Gene: SLC26A4 HGNC NCBI

Linked Data

COSMIC: COSN510705
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107674086_107674087insG , CM000669.2:g.107674086_107674087insG GRCh38
NC_000007.13:g.107314531_107314532insG , CM000669.1:g.107314531_107314532insG GRCh37
NC_000007.12:g.107101767_107101768insG NCBI36
NG_008489.1:g.18452_18453insG

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.416-78_416-77insG MANE Select ENSP00000494017.1:n.416-78_416-77insG
ENST00000265715.7:c.416-78_416-77insG ENSP00000265715.3:n.416-78_416-77insG
NM_000441.1:c.416-78_416-77insG NP_000432.1:n.416-78_416-77insG
XM_005250425.1:c.416-78_416-77insG XP_005250482.1:n.416-78_416-77insG
XM_006716025.2:c.416-78_416-77insG XP_006716088.1:n.416-78_416-77insG
XM_005250425.2:c.416-78_416-77insG XP_005250482.1:n.416-78_416-77insG
XM_006716025.3:c.416-78_416-77insG XP_006716088.1:n.416-78_416-77insG
XM_017012318.1:c.416-78_416-77insG XP_016867807.1:n.416-78_416-77insG
NM_000441.2:c.416-78_416-77insG MANE Select NP_000432.1:n.416-78_416-77insG
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