Canonical Allele Identifier: CA2676773922
Gene: PROP1 HGNC NCBI

Linked Data

gnomAD v4: 5-177992530-CCT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177992532_177992533del , CM000667.2:g.177992532_177992533del GRCh38
NC_000005.9:g.177419533_177419534del , CM000667.1:g.177419533_177419534del GRCh37
NC_000005.8:g.177352139_177352140del NCBI36
NG_015889.1:g.8711_8712del

Transcript Alleles

HGVS Amino-acid Change
ENST00000308304.2:c.*177_*178del MANE Select ENSP00000311290.2:n.*177_*178del
NM_006261.4:c.*177_*178del NP_006252.3:n.*177_*178del
NM_006261.5:c.*177_*178del MANE Select NP_006252.4:n.*177_*178del
Search 100 bp 5'
Search 100 bp 3'