Canonical Allele Identifier: CA608741268
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1368053709
gnomAD v2: 13-28498934-C-CAGTTA
gnomAD v3: 13-27924797-C-CAGTTA
gnomAD v4: 13-27924797-C-CAGTTA
MyVariant Identifiers: chr13:g.28498934_28498935insAGTTA (hg19) chr13:g.27924797_27924798insAGTTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924801_27924802insAAGTT , CM000675.2:g.27924801_27924802insAAGTT GRCh38
NC_000013.10:g.28498938_28498939insAAGTT , CM000675.1:g.28498938_28498939insAAGTT GRCh37
NC_000013.9:g.27396938_27396939insAAGTT NCBI36
NG_008183.1:g.9771_9772insAAGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*100_*101insAAGTT MANE Select ENSP00000370421.4:n.*100_*101insAAGTT
ENST00000381033.4:c.*100_*101insAAGTT ENSP00000370421.4:n.*100_*101insAAGTT
NM_000209.3:c.*100_*101insAAGTT NP_000200.1:n.*100_*101insAAGTT
NM_000209.4:c.*100_*101insAAGTT MANE Select NP_000200.1:n.*100_*101insAAGTT
Search 100 bp 5'
Search 100 bp 3'