Canonical Allele Identifier: CA1732751377
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710162_107710174delinsTGAAATCTCAAGA , CM000669.2:g.107710162_107710174delinsTGAAATCTCAAGA GRCh38
NC_000007.13:g.107350607_107350619delinsTGAAATCTCAAGA , CM000669.1:g.107350607_107350619delinsTGAAATCTCAAGA GRCh37
NC_000007.12:g.107137843_107137855delinsTGAAATCTCAAGA NCBI36
NG_008489.1:g.54528_54540delinsTGAAATCTCAAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2198_2210delinsTGAAATCTCAAGA MANE Select ENSP00000494017.1:p.Val733=
ENST00000644846.1:c.854_866delinsTGAAATCTCAAGA
ENST00000265715.7:c.2198_2210delinsTGAAATCTCAAGA ENSP00000265715.3:p.Val733=
ENST00000492030.2:n.384_396delinsTGAAATCTCAAGA
NM_000441.1:c.2198_2210delinsTGAAATCTCAAGA NP_000432.1:p.Val733=
XM_005250425.1:c.2198_2210delinsTGAAATCTCAAGA XP_005250482.1:p.Val733=
XM_005250425.2:c.2198_2210delinsTGAAATCTCAAGA XP_005250482.1:p.Val733=
XM_017012318.1:c.2120_2132delinsTGAAATCTCAAGA XP_016867807.1:p.Val707=
NM_000441.2:c.2198_2210delinsTGAAATCTCAAGA MANE Select NP_000432.1:p.Val733=