Canonical Allele Identifier: CA1732753075
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107695942G= , CM000669.2:g.107695942G= GRCh38
NC_000007.13:g.107336387G= , CM000669.1:g.107336387G= GRCh37
NC_000007.12:g.107123623G= NCBI36
NG_008489.1:g.40308G=

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1447G= MANE Select ENSP00000494017.1:p.Val483=
ENST00000644846.1:c.158G=
ENST00000265715.7:c.1447G= ENSP00000265715.3:p.Val483=
ENST00000460748.1:n.550G=
ENST00000477350.5:n.294G=
ENST00000480841.5:n.296G=
ENST00000497446.5:n.462G=
NM_000441.1:c.1447G= NP_000432.1:p.Val483=
XM_005250425.1:c.1447G= XP_005250482.1:p.Val483=
XM_005250425.2:c.1447G= XP_005250482.1:p.Val483=
XM_017012318.1:c.1369G= XP_016867807.1:p.Val457=
NM_000441.2:c.1447G= MANE Select NP_000432.1:p.Val483=