Canonical Allele Identifier: CA1732759066
Gene: SLC26A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701808_107701809delinsCA , CM000669.2:g.107701808_107701809delinsCA GRCh38
NC_000007.13:g.107342253_107342254delinsCA , CM000669.1:g.107342253_107342254delinsCA GRCh37
NC_000007.12:g.107129489_107129490delinsCA NCBI36
NG_008489.1:g.46174_46175delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1804-19_1804-18delinsCA MANE Select ENSP00000494017.1:n.1804-19_1804-18delins...
ENST00000644846.1:c.515-19_515-18delinsCA
ENST00000265715.7:c.1804-19_1804-18delinsCA ENSP00000265715.3:n.1804-19_1804-18delins...
ENST00000480841.5:n.653-19_653-18delinsCA
ENST00000492030.2:n.91-19_91-18delinsCA
NM_000441.1:c.1804-19_1804-18delinsCA NP_000432.1:n.1804-19_1804-18delinsCA
XM_005250425.1:c.1804-19_1804-18delinsCA XP_005250482.1:n.1804-19_1804-18delinsCA
XM_005250425.2:c.1804-19_1804-18delinsCA XP_005250482.1:n.1804-19_1804-18delinsCA
XM_017012318.1:c.1726-19_1726-18delinsCA XP_016867807.1:n.1726-19_1726-18delinsCA
NM_000441.2:c.1804-19_1804-18delinsCA MANE Select NP_000432.1:n.1804-19_1804-18delinsCA