Canonical Allele Identifier: CA2578988563
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107663234G>A , CM000669.2:g.107663234G>A GRCh38
NC_000007.13:g.107303679G>A , CM000669.1:g.107303679G>A GRCh37
NC_000007.12:g.107090915G>A NCBI36
NG_008489.1:g.7600G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.165-62G>A MANE Select ENSP00000494017.1:n.165-62G>A
ENST00000265715.7:c.165-62G>A ENSP00000265715.3:n.165-62G>A
ENST00000440056.1:c.165-62G>A ENSP00000394760.1:n.165-62G>A
NM_000441.1:c.165-62G>A NP_000432.1:n.165-62G>A
XM_005250425.1:c.165-62G>A XP_005250482.1:n.165-62G>A
XM_006716025.2:c.165-62G>A XP_006716088.1:n.165-62G>A
XM_005250425.2:c.165-62G>A XP_005250482.1:n.165-62G>A
XM_006716025.3:c.165-62G>A XP_006716088.1:n.165-62G>A
XM_017012318.1:c.165-62G>A XP_016867807.1:n.165-62G>A
NM_000441.2:c.165-62G>A MANE Select NP_000432.1:n.165-62G>A
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