Canonical Allele Identifier: CA2675943663
Gene: SLC26A2 HGNC NCBI

Linked Data

gnomAD v4: 5-149981816-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.149981817del , CM000667.2:g.149981817del GRCh38
NC_000005.9:g.149361380del , CM000667.1:g.149361380del GRCh37
NC_000005.8:g.149341573del NCBI36
NG_007147.2:g.22935del , LRG_684:g.22935del

Transcript Alleles

HGVS Amino-acid Change
ENST00000286298.5:c.*4del MANE Select ENSP00000286298.4:n.*4del
ENST00000286298.4:c.*4del ENSP00000286298.4:n.*4del
ENST00000503336.1:c.372+3466del ENSP00000426053.1:n.372+3466del
NM_000112.3:c.*4del , LRG_684t1:c.*4del NP_000103.2:n.*4del
XM_017009191.2:c.*4del XP_016864680.1:n.*4del
NM_000112.4:c.*4del MANE Select NP_000103.2:n.*4del
Search 100 bp 5'
Search 100 bp 3'