Canonical Allele Identifier: CA564901103
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1194693018
gnomAD v2: 5-177420096-G-GTGACACCCTATGTCAA
gnomAD v4: 5-177993095-G-GTGACACCCTATGTCAA
MyVariant Identifiers: chr5:g.177420096_177420097insTGACACCCTATGTCAA (hg19) chr5:g.177993095_177993096insTGACACCCTATGTCAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177993105_177993106insTGTCAATGACACCCTA , CM000667.2:g.177993105_177993106insTGTCAATGACACCCTA GRCh38
NC_000005.9:g.177420106_177420107insTGTCAATGACACCCTA , CM000667.1:g.177420106_177420107insTGTCAATGACACCCTA GRCh37
NC_000005.8:g.177352712_177352713insTGTCAATGACACCCTA NCBI36
NG_015889.1:g.8147_8148insTTGACATAGGGTGTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.343-49_343-48insTTGACATAGGGTGTCA MANE Select ENSP00000311290.2:n.343-49_343-48insTTGACATAGGGTGTCA
NM_006261.4:c.343-49_343-48insTTGACATAGGGTGTCA NP_006252.3:n.343-49_343-48insTTGACATAGGGTGTCA
NM_006261.5:c.343-49_343-48insTTGACATAGGGTGTCA MANE Select NP_006252.4:n.343-49_343-48insTTGACATAGGGTGTCA
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