Canonical Allele Identifier: CA2676773885
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992516-A-ACCCCTACAGCCATGCCCTC
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992518_177992519insCCTACAGCCATGCCCTCCC , CM000667.2:g.177992518_177992519insCCTACAGCCATGCCCTCCC GRCh38
NC_000005.9:g.177419519_177419520insCCTACAGCCATGCCCTCCC , CM000667.1:g.177419519_177419520insCCTACAGCCATGCCCTCCC GRCh37
NC_000005.8:g.177352125_177352126insCCTACAGCCATGCCCTCCC NCBI36
NG_015889.1:g.8726_8727insGAGGGCATGGCTGTAGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*192_*193insGAGGGCATGGCTGTAGGGG MANE Select ENSP00000311290.2:n.*192_*193insGAGGGCATGGCTGTAGGGG
NM_006261.4:c.*192_*193insGAGGGCATGGCTGTAGGGG NP_006252.3:n.*192_*193insGAGGGCATGGCTGTAGGGG
NM_006261.5:c.*192_*193insGAGGGCATGGCTGTAGGGG MANE Select NP_006252.4:n.*192_*193insGAGGGCATGGCTGTAGGGG
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