Canonical Allele Identifier: CA2525508283
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701030C>T , CM000669.2:g.107701030C>T GRCh38
NC_000007.13:g.107341475C>T , CM000669.1:g.107341475C>T GRCh37
NC_000007.12:g.107128711C>T NCBI36
NG_008489.1:g.45396C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1708-71C>T MANE Select ENSP00000494017.1:n.1708-71C>T
ENST00000644846.1:c.419-71C>T
ENST00000265715.7:c.1708-71C>T ENSP00000265715.3:n.1708-71C>T
ENST00000480841.5:n.557-71C>T
ENST00000492030.2:n.91-797C>T
NM_000441.1:c.1708-71C>T NP_000432.1:n.1708-71C>T
XM_005250425.1:c.1708-71C>T XP_005250482.1:n.1708-71C>T
XM_005250425.2:c.1708-71C>T XP_005250482.1:n.1708-71C>T
XM_017012318.1:c.1630-71C>T XP_016867807.1:n.1630-71C>T
NM_000441.2:c.1708-71C>T MANE Select NP_000432.1:n.1708-71C>T