Canonical Allele Identifier: CA1732756959
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717310G= , CM000669.2:g.107717310G= GRCh38
NC_000007.13:g.107357755G= , CM000669.1:g.107357755G= GRCh37
NC_000007.12:g.107144991G= NCBI36
NG_008489.1:g.61676G=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1864G= MANE Select ENSP00000494017.1:n.*1864G=
ENST00000644846.1:c.2863G=
ENST00000265715.7:c.*1864G= ENSP00000265715.3:n.*1864G=
NM_000441.1:c.*1864G= NP_000432.1:n.*1864G=
NM_000441.2:c.*1864G= MANE Select NP_000432.1:n.*1864G=