Canonical Allele Identifier: CA1105620959
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v3: 7-107701770-ATGGT-A
gnomAD v4: 7-107701770-ATGGT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701773_107701776del , CM000669.2:g.107701773_107701776del GRCh38
NC_000007.13:g.107342218_107342221del , CM000669.1:g.107342218_107342221del GRCh37
NC_000007.12:g.107129454_107129457del NCBI36
NG_008489.1:g.46139_46142del

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1804-54_1804-51del MANE Select ENSP00000494017.1:n.1804-54_1804-51del
ENST00000644846.1:c.515-54_515-51del
ENST00000265715.7:c.1804-54_1804-51del ENSP00000265715.3:n.1804-54_1804-51del
ENST00000480841.5:n.653-54_653-51del
ENST00000492030.2:n.91-54_91-51del
NM_000441.1:c.1804-54_1804-51del NP_000432.1:n.1804-54_1804-51del
XM_005250425.1:c.1804-54_1804-51del XP_005250482.1:n.1804-54_1804-51del
XM_005250425.2:c.1804-54_1804-51del XP_005250482.1:n.1804-54_1804-51del
XM_017012318.1:c.1726-54_1726-51del XP_016867807.1:n.1726-54_1726-51del
NM_000441.2:c.1804-54_1804-51del MANE Select NP_000432.1:n.1804-54_1804-51del
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