Canonical Allele Identifier: CA1732758198
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701038_107701039delinsCA , CM000669.2:g.107701038_107701039delinsCA GRCh38
NC_000007.13:g.107341483_107341484delinsCA , CM000669.1:g.107341483_107341484delinsCA GRCh37
NC_000007.12:g.107128719_107128720delinsCA NCBI36
NG_008489.1:g.45404_45405delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1708-63_1708-62delinsCA MANE Select ENSP00000494017.1:n.1708-63_1708-62delins...
ENST00000644846.1:c.419-63_419-62delinsCA
ENST00000265715.7:c.1708-63_1708-62delinsCA ENSP00000265715.3:n.1708-63_1708-62delins...
ENST00000480841.5:n.557-63_557-62delinsCA
ENST00000492030.2:n.91-789_91-788delinsCA
NM_000441.1:c.1708-63_1708-62delinsCA NP_000432.1:n.1708-63_1708-62delinsCA
XM_005250425.1:c.1708-63_1708-62delinsCA XP_005250482.1:n.1708-63_1708-62delinsCA
XM_005250425.2:c.1708-63_1708-62delinsCA XP_005250482.1:n.1708-63_1708-62delinsCA
XM_017012318.1:c.1630-63_1630-62delinsCA XP_016867807.1:n.1630-63_1630-62delinsCA
NM_000441.2:c.1708-63_1708-62delinsCA MANE Select NP_000432.1:n.1708-63_1708-62delinsCA