Canonical Allele Identifier: CA564901148
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1554182366
gnomAD v2: 5-177419755-A-AGGGGGGGGGGGGGGGGGGGGG
gnomAD v3: 5-177992754-A-AGGGGGGGGGGGGGGGGGGGGG
gnomAD v4: 5-177992754-A-AGGGGGGGGGGGGGGGGGGGGG
MyVariant Identifiers: chr5:g.177419755_177419756insGGGGGGGGGGGGGGGGGGGGG (hg19) chr5:g.177992754_177992755insGGGGGGGGGGGGGGGGGGGGG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992759_177992760insGGGGGGGGGGGGGGGGGGGGG , CM000667.2:g.177992759_177992760insGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000005.9:g.177419760_177419761insGGGGGGGGGGGGGGGGGGGGG , CM000667.1:g.177419760_177419761insGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000005.8:g.177352366_177352367insGGGGGGGGGGGGGGGGGGGGG NCBI36
NG_015889.1:g.8488_8489insCCCCCCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.635_636insCCCCCCCCCCCCCCCCCCCCC MANE Select ENSP00000311290.2:p.Pro212_Pro213insProProProProProProPro
NM_006261.4:c.635_636insCCCCCCCCCCCCCCCCCCCCC NP_006252.3:p.Pro212_Pro213insProProProProProProPro
NM_006261.5:c.635_636insCCCCCCCCCCCCCCCCCCCCC MANE Select NP_006252.4:p.Pro212_Pro213insProProProProProProPro
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