Canonical Allele Identifier: CA564507217
Gene: PROP1 HGNC NCBI

Linked Data

dbSNP Id: rs1466775126
gnomAD v2: 5-177419572-A-AT
gnomAD v3: 5-177992571-A-AT
gnomAD v4: 5-177992571-A-AT
MyVariant Identifiers: chr5:g.177419572_177419573insT (hg19) chr5:g.177992571_177992572insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992576dup , CM000667.2:g.177992576dup GRCh38
NC_000005.9:g.177419577dup , CM000667.1:g.177419577dup GRCh37
NC_000005.8:g.177352183dup NCBI36
NG_015889.1:g.8671dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*137dup MANE Select ENSP00000311290.2:n.*137dup
NM_006261.4:c.*137dup NP_006252.3:n.*137dup
NM_006261.5:c.*137dup MANE Select NP_006252.4:n.*137dup
Search 100 bp 5'
Search 100 bp 3'