Canonical Allele Identifier: CA1732751341
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710132A= , CM000669.2:g.107710132A= GRCh38
NC_000007.13:g.107350577A= , CM000669.1:g.107350577A= GRCh37
NC_000007.12:g.107137813A= NCBI36
NG_008489.1:g.54498A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2168A= MANE Select ENSP00000494017.1:p.His723=
ENST00000644846.1:c.824A=
ENST00000265715.7:c.2168A= ENSP00000265715.3:p.His723=
ENST00000492030.2:n.377-23A=
NM_000441.1:c.2168A= NP_000432.1:p.His723=
XM_005250425.1:c.2168A= XP_005250482.1:p.His723=
XM_005250425.2:c.2168A= XP_005250482.1:p.His723=
XM_017012318.1:c.2090A= XP_016867807.1:p.His697=
NM_000441.2:c.2168A= MANE Select NP_000432.1:p.His723=