Canonical Allele Identifier: CA1732751405
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710187_107710188delinsCA , CM000669.2:g.107710187_107710188delinsCA GRCh38
NC_000007.13:g.107350632_107350633delinsCA , CM000669.1:g.107350632_107350633delinsCA GRCh37
NC_000007.12:g.107137868_107137869delinsCA NCBI36
NG_008489.1:g.54553_54554delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2223_2224delinsCA MANE Select ENSP00000494017.1:p.Ser741=
ENST00000644846.1:c.879_880delinsCA
ENST00000265715.7:c.2223_2224delinsCA ENSP00000265715.3:p.Ser741=
ENST00000492030.2:n.409_410delinsCA
NM_000441.1:c.2223_2224delinsCA NP_000432.1:p.Ser741=
XM_005250425.1:c.2223_2224delinsCA XP_005250482.1:p.Ser741=
XM_005250425.2:c.2223_2224delinsCA XP_005250482.1:p.Ser741=
XM_017012318.1:c.2145_2146delinsCA XP_016867807.1:p.Ser715=
NM_000441.2:c.2223_2224delinsCA MANE Select NP_000432.1:p.Ser741=