Canonical Allele Identifier: CA368841200
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107695943T>G , CM000669.2:g.107695943T>G GRCh38
NC_000007.13:g.107336388T>G , CM000669.1:g.107336388T>G GRCh37
NC_000007.12:g.107123624T>G NCBI36
NG_008489.1:g.40309T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1448T>G MANE Select ENSP00000494017.1:p.Val483Gly
ENST00000644846.1:c.159T>G
ENST00000265715.7:c.1448T>G ENSP00000265715.3:p.Val483Gly
ENST00000460748.1:n.551T>G
ENST00000477350.5:n.295T>G
ENST00000480841.5:n.297T>G
ENST00000497446.5:n.463T>G
NM_000441.1:c.1448T>G NP_000432.1:p.Val483Gly
XM_005250425.1:c.1448T>G XP_005250482.1:p.Val483Gly
XM_005250425.2:c.1448T>G XP_005250482.1:p.Val483Gly
XM_017012318.1:c.1370T>G XP_016867807.1:p.Val457Gly
NM_000441.2:c.1448T>G MANE Select NP_000432.1:p.Val483Gly