Canonical Allele Identifier: CA2615682177
Gene: PGR HGNC NCBI
PGR-AS1 HGNC NCBI

Linked Data

gnomAD v4: 11-101129483-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101129486del , CM000673.2:g.101129486del GRCh38
NC_000011.9:g.101000217del , CM000673.1:g.101000217del GRCh37
NC_000011.8:g.100505427del NCBI36
NG_016475.1:g.5330del

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.-414del (PGR) MANE Select ENSP00000325120.5:n.-414del
ENST00000325455.9:c.-414del (PGR) ENSP00000325120.5:n.-414del
ENST00000534013.5:c.-202del (PGR) ENSP00000436561.1:n.-202del
ENST00000617858.4:c.-414del (PGR) ENSP00000481227.1:n.-414del
ENST00000619228.2:c.-414del (PGR) ENSP00000482698.1:n.-414del
NM_000926.4:c.-414del (PGR) MANE Select NP_000917.3:n.-414del
NM_001271162.1:c.-202del (PGR) NP_001258091.1:n.-202del
NR_073144.1:n.410del (PGR-AS1)
XM_006718858.2:c.-414del (PGR) XP_006718921.1:n.-414del
XM_011542869.1:c.-414del (PGR) XP_011541171.1:n.-414del
XR_947831.1:n.1159del (PGR)
XM_006718858.3:c.-414del (PGR) XP_006718921.1:n.-414del
XM_011542869.2:c.-414del (PGR) XP_011541171.1:n.-414del
NM_001271162.2:c.-202del (PGR) NP_001258091.1:n.-202del
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