Canonical Allele Identifier: CA1732755276
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107698070C= , CM000669.2:g.107698070C= GRCh38
NC_000007.13:g.107338515C= , CM000669.1:g.107338515C= GRCh37
NC_000007.12:g.107125751C= NCBI36
NG_008489.1:g.42436C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1573C= MANE Select ENSP00000494017.1:p.Pro525=
ENST00000644846.1:c.284C=
ENST00000265715.7:c.1573C= ENSP00000265715.3:p.Pro525=
ENST00000477350.5:n.420C=
ENST00000480841.5:n.422C=
NM_000441.1:c.1573C= NP_000432.1:p.Pro525=
XM_005250425.1:c.1573C= XP_005250482.1:p.Pro525=
XM_005250425.2:c.1573C= XP_005250482.1:p.Pro525=
XM_017012318.1:c.1495C= XP_016867807.1:p.Pro499=
NM_000441.2:c.1573C= MANE Select NP_000432.1:p.Pro525=