Canonical Allele Identifier: CA1732758129
Gene: SLC26A4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107700961C= , CM000669.2:g.107700961C= GRCh38
NC_000007.13:g.107341406C= , CM000669.1:g.107341406C= GRCh37
NC_000007.12:g.107128642C= NCBI36
NG_008489.1:g.45327C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1708-140C= MANE Select ENSP00000494017.1:n.1708-140C=
ENST00000644846.1:c.419-140C=
ENST00000265715.7:c.1708-140C= ENSP00000265715.3:n.1708-140C=
ENST00000480841.5:n.557-140C=
ENST00000492030.2:n.90+786C=
NM_000441.1:c.1708-140C= NP_000432.1:n.1708-140C=
XM_005250425.1:c.1708-140C= XP_005250482.1:n.1708-140C=
XM_005250425.2:c.1708-140C= XP_005250482.1:n.1708-140C=
XM_017012318.1:c.1630-140C= XP_016867807.1:n.1630-140C=
NM_000441.2:c.1708-140C= MANE Select NP_000432.1:n.1708-140C=
Search 100 bp 5'
Search 100 bp 3'