Canonical Allele Identifier: CA457104605
Gene: SLC26A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107350575C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710130C>T , CM000669.2:g.107710130C>T GRCh38
NC_000007.13:g.107350575C>T , CM000669.1:g.107350575C>T GRCh37
NC_000007.12:g.107137811C>T NCBI36
NG_008489.1:g.54496C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2166C>T MANE Select ENSP00000494017.1:p.Val722=
ENST00000644846.1:c.822C>T
ENST00000265715.7:c.2166C>T ENSP00000265715.3:p.Val722=
ENST00000492030.2:n.377-25C>T
NM_000441.1:c.2166C>T NP_000432.1:p.Val722=
XM_005250425.1:c.2166C>T XP_005250482.1:p.Val722=
XM_005250425.2:c.2166C>T XP_005250482.1:p.Val722=
XM_017012318.1:c.2088C>T XP_016867807.1:p.Val696=
NM_000441.2:c.2166C>T MANE Select NP_000432.1:p.Val722=