Canonical Allele Identifier: CA1732755797
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107716012C= , CM000669.2:g.107716012C= GRCh38
NC_000007.13:g.107356457C= , CM000669.1:g.107356457C= GRCh37
NC_000007.12:g.107143693C= NCBI36
NG_008489.1:g.60378C=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*566C= MANE Select ENSP00000494017.1:n.*566C=
ENST00000644846.1:c.1565C=
ENST00000265715.7:c.*566C= ENSP00000265715.3:n.*566C=
NM_000441.1:c.*566C= NP_000432.1:n.*566C=
XM_005250425.2:c.*566C= XP_005250482.1:n.*566C=
XM_017012318.1:c.*566C= XP_016867807.1:n.*566C=
NM_000441.2:c.*566C= MANE Select NP_000432.1:n.*566C=