Canonical Allele Identifier: CA2684467606
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107694473_107694490del , CM000669.2:g.107694473_107694490del GRCh38
NC_000007.13:g.107334918_107334935del , CM000669.1:g.107334918_107334935del GRCh37
NC_000007.12:g.107122154_107122171del NCBI36
NG_008489.1:g.38839_38856del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1334_1341+10del
ENST00000644846.1:c.45_52+10del
ENST00000265715.7:c.1334_1341+10del
ENST00000460748.1:n.437_444+10del
ENST00000477350.5:n.189-148_189-131del
ENST00000480841.5:n.183_190+10del
ENST00000497446.5:n.349_356+10del
NM_000441.1:c.1334_1341+10del
XM_005250425.1:c.1334_1341+10del
XM_005250425.2:c.1334_1341+10del
XM_017012318.1:c.1264-148_1264-131del XP_016867807.1:n.1264-148_1264-131del
NM_000441.2:c.1334_1341+10del