Canonical Allele Identifier: CA1732751340
Gene: SLC26A4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107694400C= , CM000669.2:g.107694400C= GRCh38
NC_000007.13:g.107334845C= , CM000669.1:g.107334845C= GRCh37
NC_000007.12:g.107122081C= NCBI36
NG_008489.1:g.38766C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1264-3C= MANE Select ENSP00000494017.1:n.1264-3C=
ENST00000265715.7:c.1264-3C= ENSP00000265715.3:n.1264-3C=
ENST00000460748.1:n.367-3C=
ENST00000477350.5:n.189-221C=
ENST00000480841.5:n.113-3C=
ENST00000497446.5:n.279-3C=
NM_000441.1:c.1264-3C= NP_000432.1:n.1264-3C=
XM_005250425.1:c.1264-3C= XP_005250482.1:n.1264-3C=
XM_005250425.2:c.1264-3C= XP_005250482.1:n.1264-3C=
XM_017012318.1:c.1264-221C= XP_016867807.1:n.1264-221C=
NM_000441.2:c.1264-3C= MANE Select NP_000432.1:n.1264-3C=
Search 100 bp 5'
Search 100 bp 3'