Canonical Allele Identifier: CA1732755799
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107716013G= , CM000669.2:g.107716013G= GRCh38
NC_000007.13:g.107356458G= , CM000669.1:g.107356458G= GRCh37
NC_000007.12:g.107143694G= NCBI36
NG_008489.1:g.60379G=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*567G= MANE Select ENSP00000494017.1:n.*567G=
ENST00000644846.1:c.1566G=
ENST00000265715.7:c.*567G= ENSP00000265715.3:n.*567G=
NM_000441.1:c.*567G= NP_000432.1:n.*567G=
XM_005250425.2:c.*567G= XP_005250482.1:n.*567G=
XM_017012318.1:c.*567G= XP_016867807.1:n.*567G=
NM_000441.2:c.*567G= MANE Select NP_000432.1:n.*567G=