Canonical Allele Identifier: CA457104738
Gene: SLC26A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107350632C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710187C>G , CM000669.2:g.107710187C>G GRCh38
NC_000007.13:g.107350632C>G , CM000669.1:g.107350632C>G GRCh37
NC_000007.12:g.107137868C>G NCBI36
NG_008489.1:g.54553C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2223C>G MANE Select ENSP00000494017.1:p.Ser741=
ENST00000644846.1:c.879C>G
ENST00000265715.7:c.2223C>G ENSP00000265715.3:p.Ser741=
ENST00000492030.2:n.409C>G
NM_000441.1:c.2223C>G NP_000432.1:p.Ser741=
XM_005250425.1:c.2223C>G XP_005250482.1:p.Ser741=
XM_005250425.2:c.2223C>G XP_005250482.1:p.Ser741=
XM_017012318.1:c.2145C>G XP_016867807.1:p.Ser715=
NM_000441.2:c.2223C>G MANE Select NP_000432.1:p.Ser741=