Canonical Allele Identifier: CA608987662
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1212668172
gnomAD v2: 13-28498430-GACGCGCACGGCCTAC-G
gnomAD v3: 13-27924293-GACGCGCACGGCCTAC-G
gnomAD v4: 13-27924293-GACGCGCACGGCCTAC-G
MyVariant Identifiers: chr13:g.28498431_28498445del (hg19) chr13:g.27924294_27924308del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924300_27924314del , CM000675.2:g.27924300_27924314del GRCh38
NC_000013.10:g.28498437_28498451del , CM000675.1:g.28498437_28498451del GRCh37
NC_000013.9:g.27396437_27396451del NCBI36
NG_008183.1:g.9270_9284del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.451_465del MANE Select ENSP00000370421.4:p.Thr151_Arg155del
ENST00000381033.4:c.451_465del ENSP00000370421.4:p.Thr151_Arg155del
NM_000209.3:c.451_465del NP_000200.1:p.Thr151_Arg155del
XR_941579.1:n.2177_2191del
XR_941580.1:n.1093_1107del
XR_941580.2:n.1105_1119del
NM_000209.4:c.451_465del MANE Select NP_000200.1:p.Thr151_Arg155del
Search 100 bp 5'
Search 100 bp 3'