Canonical Allele Identifier: CA368843522
Gene: SLC26A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107342380G>C (hg19) chr7:g.107701935G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701935G>C , CM000669.2:g.107701935G>C GRCh38
NC_000007.13:g.107342380G>C , CM000669.1:g.107342380G>C GRCh37
NC_000007.12:g.107129616G>C NCBI36
NG_008489.1:g.46301G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1912G>C MANE Select ENSP00000494017.1:p.Val638Leu
ENST00000644846.1:c.623G>C
ENST00000265715.7:c.1912G>C ENSP00000265715.3:p.Val638Leu
ENST00000492030.2:n.199G>C
NM_000441.1:c.1912G>C NP_000432.1:p.Val638Leu
XM_005250425.1:c.1912G>C XP_005250482.1:p.Val638Leu
XM_005250425.2:c.1912G>C XP_005250482.1:p.Val638Leu
XM_017012318.1:c.1834G>C XP_016867807.1:p.Val612Leu
NM_000441.2:c.1912G>C MANE Select NP_000432.1:p.Val638Leu
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