Canonical Allele Identifier: CA2684469049
Gene: SLC26A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701817del , CM000669.2:g.107701817del GRCh38
NC_000007.13:g.107342262del , CM000669.1:g.107342262del GRCh37
NC_000007.12:g.107129498del NCBI36
NG_008489.1:g.46183del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1804-10del MANE Select ENSP00000494017.1:n.1804-10del
ENST00000644846.1:c.515-10del
ENST00000265715.7:c.1804-10del ENSP00000265715.3:n.1804-10del
ENST00000480841.5:n.653-10del
ENST00000492030.2:n.91-10del
NM_000441.1:c.1804-10del NP_000432.1:n.1804-10del
XM_005250425.1:c.1804-10del XP_005250482.1:n.1804-10del
XM_005250425.2:c.1804-10del XP_005250482.1:n.1804-10del
XM_017012318.1:c.1726-10del XP_016867807.1:n.1726-10del
NM_000441.2:c.1804-10del MANE Select NP_000432.1:n.1804-10del