Canonical Allele Identifier: CA457104608
Gene: SLC26A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107350584T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710139T>A , CM000669.2:g.107710139T>A GRCh38
NC_000007.13:g.107350584T>A , CM000669.1:g.107350584T>A GRCh37
NC_000007.12:g.107137820T>A NCBI36
NG_008489.1:g.54505T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2175T>A MANE Select ENSP00000494017.1:p.Ala725=
ENST00000644846.1:c.831T>A
ENST00000265715.7:c.2175T>A ENSP00000265715.3:p.Ala725=
ENST00000492030.2:n.377-16T>A
NM_000441.1:c.2175T>A NP_000432.1:p.Ala725=
XM_005250425.1:c.2175T>A XP_005250482.1:p.Ala725=
XM_005250425.2:c.2175T>A XP_005250482.1:p.Ala725=
XM_017012318.1:c.2097T>A XP_016867807.1:p.Ala699=
NM_000441.2:c.2175T>A MANE Select NP_000432.1:p.Ala725=