Canonical Allele Identifier: CA457102002
Gene: SLC26A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107341569A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701124A>C , CM000669.2:g.107701124A>C GRCh38
NC_000007.13:g.107341569A>C , CM000669.1:g.107341569A>C GRCh37
NC_000007.12:g.107128805A>C NCBI36
NG_008489.1:g.45490A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1731A>C MANE Select ENSP00000494017.1:p.Val577=
ENST00000644846.1:c.442A>C
ENST00000265715.7:c.1731A>C ENSP00000265715.3:p.Val577=
ENST00000480841.5:n.580A>C
ENST00000492030.2:n.91-703A>C
NM_000441.1:c.1731A>C NP_000432.1:p.Val577=
XM_005250425.1:c.1731A>C XP_005250482.1:p.Val577=
XM_005250425.2:c.1731A>C XP_005250482.1:p.Val577=
XM_017012318.1:c.1653A>C XP_016867807.1:p.Val551=
NM_000441.2:c.1731A>C MANE Select NP_000432.1:p.Val577=
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