Canonical Allele Identifier: CA1732751315
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710117T= , CM000669.2:g.107710117T= GRCh38
NC_000007.13:g.107350562T= , CM000669.1:g.107350562T= GRCh37
NC_000007.12:g.107137798T= NCBI36
NG_008489.1:g.54483T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2153T= MANE Select ENSP00000494017.1:p.Phe718=
ENST00000644846.1:c.809T=
ENST00000265715.7:c.2153T= ENSP00000265715.3:p.Phe718=
ENST00000492030.2:n.377-38T=
NM_000441.1:c.2153T= NP_000432.1:p.Phe718=
XM_005250425.1:c.2153T= XP_005250482.1:p.Phe718=
XM_005250425.2:c.2153T= XP_005250482.1:p.Phe718=
XM_017012318.1:c.2075T= XP_016867807.1:p.Phe692=
NM_000441.2:c.2153T= MANE Select NP_000432.1:p.Phe718=