Canonical Allele Identifier: CA1732755792
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107716008T= , CM000669.2:g.107716008T= GRCh38
NC_000007.13:g.107356453T= , CM000669.1:g.107356453T= GRCh37
NC_000007.12:g.107143689T= NCBI36
NG_008489.1:g.60374T=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*562T= MANE Select ENSP00000494017.1:n.*562T=
ENST00000644846.1:c.1561T=
ENST00000265715.7:c.*562T= ENSP00000265715.3:n.*562T=
NM_000441.1:c.*562T= NP_000432.1:n.*562T=
XM_005250425.2:c.*562T= XP_005250482.1:n.*562T=
XM_017012318.1:c.*562T= XP_016867807.1:n.*562T=
NM_000441.2:c.*562T= MANE Select NP_000432.1:n.*562T=