Canonical Allele Identifier: CA1732750858
Gene: SLC26A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107709746A= , CM000669.2:g.107709746A= GRCh38
NC_000007.13:g.107350191A= , CM000669.1:g.107350191A= GRCh37
NC_000007.12:g.107137427A= NCBI36
NG_008489.1:g.54112A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2090-308A= MANE Select ENSP00000494017.1:n.2090-308A=
ENST00000644846.1:c.746-308A=
ENST00000265715.7:c.2090-308A= ENSP00000265715.3:n.2090-308A=
ENST00000492030.2:n.377-409A=
NM_000441.1:c.2090-308A= NP_000432.1:n.2090-308A=
XM_005250425.1:c.2090-308A= XP_005250482.1:n.2090-308A=
XM_005250425.2:c.2090-308A= XP_005250482.1:n.2090-308A=
XM_017012318.1:c.2012-308A= XP_016867807.1:n.2012-308A=
NM_000441.2:c.2090-308A= MANE Select NP_000432.1:n.2090-308A=
Search 100 bp 5'
Search 100 bp 3'