Canonical Allele Identifier: CA1732757195
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717485T= , CM000669.2:g.107717485T= GRCh38
NC_000007.13:g.107357930T= , CM000669.1:g.107357930T= GRCh37
NC_000007.12:g.107145166T= NCBI36
NG_008489.1:g.61851T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.*2039T= MANE Select ENSP00000494017.1:n.*2039T=
ENST00000265715.7:c.*2039T= ENSP00000265715.3:n.*2039T=
NM_000441.1:c.*2039T= NP_000432.1:n.*2039T=
NM_000441.2:c.*2039T= MANE Select NP_000432.1:n.*2039T=