Canonical Allele Identifier: CA2676774215
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992655-G-GT
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992656dup , CM000667.2:g.177992656dup GRCh38
NC_000005.9:g.177419657dup , CM000667.1:g.177419657dup GRCh37
NC_000005.8:g.177352263dup NCBI36
NG_015889.1:g.8587dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*53dup MANE Select ENSP00000311290.2:n.*53dup
NM_006261.4:c.*53dup NP_006252.3:n.*53dup
NM_006261.5:c.*53dup MANE Select NP_006252.4:n.*53dup
Search 100 bp 5'
Search 100 bp 3'