Canonical Allele Identifier: CA2578988916
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701802A>G , CM000669.2:g.107701802A>G GRCh38
NC_000007.13:g.107342247A>G , CM000669.1:g.107342247A>G GRCh37
NC_000007.12:g.107129483A>G NCBI36
NG_008489.1:g.46168A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1804-25A>G MANE Select ENSP00000494017.1:n.1804-25A>G
ENST00000644846.1:c.515-25A>G
ENST00000265715.7:c.1804-25A>G ENSP00000265715.3:n.1804-25A>G
ENST00000480841.5:n.653-25A>G
ENST00000492030.2:n.91-25A>G
NM_000441.1:c.1804-25A>G NP_000432.1:n.1804-25A>G
XM_005250425.1:c.1804-25A>G XP_005250482.1:n.1804-25A>G
XM_005250425.2:c.1804-25A>G XP_005250482.1:n.1804-25A>G
XM_017012318.1:c.1726-25A>G XP_016867807.1:n.1726-25A>G
NM_000441.2:c.1804-25A>G MANE Select NP_000432.1:n.1804-25A>G