Canonical Allele Identifier: CA457103234
Gene: SLC26A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107342340G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701895G>C , CM000669.2:g.107701895G>C GRCh38
NC_000007.13:g.107342340G>C , CM000669.1:g.107342340G>C GRCh37
NC_000007.12:g.107129576G>C NCBI36
NG_008489.1:g.46261G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1872G>C MANE Select ENSP00000494017.1:p.Leu624=
ENST00000644846.1:c.583G>C
ENST00000265715.7:c.1872G>C ENSP00000265715.3:p.Leu624=
ENST00000492030.2:n.159G>C
NM_000441.1:c.1872G>C NP_000432.1:p.Leu624=
XM_005250425.1:c.1872G>C XP_005250482.1:p.Leu624=
XM_005250425.2:c.1872G>C XP_005250482.1:p.Leu624=
XM_017012318.1:c.1794G>C XP_016867807.1:p.Leu598=
NM_000441.2:c.1872G>C MANE Select NP_000432.1:p.Leu624=