Canonical Allele Identifier: CA1732755795
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1792337092
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107716011C>T , CM000669.2:g.107716011C>T GRCh38
NC_000007.13:g.107356456C>T , CM000669.1:g.107356456C>T GRCh37
NC_000007.12:g.107143692C>T NCBI36
NG_008489.1:g.60377C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*565C>T MANE Select ENSP00000494017.1:n.*565C>T
ENST00000644846.1:c.1564C>T
ENST00000265715.7:c.*565C>T ENSP00000265715.3:n.*565C>T
NM_000441.1:c.*565C>T NP_000432.1:n.*565C>T
XM_005250425.2:c.*565C>T XP_005250482.1:n.*565C>T
XM_017012318.1:c.*565C>T XP_016867807.1:n.*565C>T
NM_000441.2:c.*565C>T MANE Select NP_000432.1:n.*565C>T
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