Canonical Allele Identifier: CA148446819
Gene: SGK1 HGNC NCBI

Linked Data

dbSNP Id: rs774830267
gnomAD v2: 6-134599179-AATG-A
gnomAD v3: 6-134278041-AATG-A
gnomAD v4: 6-134278041-AATG-A
MyVariant Identifiers: chr6:g.134599180_134599182del (hg19) chr6:g.134278042_134278044del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134278047_134278049del , CM000668.2:g.134278047_134278049del GRCh38
NC_000006.11:g.134599185_134599187del , CM000668.1:g.134599185_134599187del GRCh37
NC_000006.10:g.134640878_134640880del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000367858.10:c.70-15896_70-15894del MANE Select ENSP00000356832.5:n.70-15896_70-15894del
ENST00000367858.9:c.70-15896_70-15894del ENSP00000356832.5:n.70-15896_70-15894del
ENST00000461976.2:c.-24-15896_-24-15894del ENSP00000435577.1:n.-24-15896_-24-15894de...
ENST00000524929.1:c.70-15896_70-15894del ENSP00000435724.1:n.70-15896_70-15894del
ENST00000533224.1:c.70-15896_70-15894del ENSP00000436470.1:n.70-15896_70-15894del
NM_001143676.1:c.70-15896_70-15894del NP_001137148.1:n.70-15896_70-15894del
XM_011536071.1:c.70-15896_70-15894del XP_011534373.1:n.70-15896_70-15894del
NM_001143676.3:c.70-15896_70-15894del MANE Select NP_001137148.1:n.70-15896_70-15894del
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