Canonical Allele Identifier: CA2615682086
Gene: PGR HGNC NCBI
PGR-AS1 HGNC NCBI

Linked Data

gnomAD v4: 11-101129394-TTC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101129396_101129397del , CM000673.2:g.101129396_101129397del GRCh38
NC_000011.9:g.101000127_101000128del , CM000673.1:g.101000127_101000128del GRCh37
NC_000011.8:g.100505337_100505338del NCBI36
NG_016475.1:g.5418_5419del

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.-326_-325del (PGR) MANE Select ENSP00000325120.5:n.-326_-325del
ENST00000325455.9:c.-326_-325del (PGR) ENSP00000325120.5:n.-326_-325del
ENST00000534013.5:c.-146+32_-146+33del (PGR) ENSP00000436561.1:n.-146+32_-146+33del
ENST00000617858.4:c.-326_-325del (PGR) ENSP00000481227.1:n.-326_-325del
ENST00000619228.2:c.-326_-325del (PGR) ENSP00000482698.1:n.-326_-325del
NM_000926.4:c.-326_-325del (PGR) MANE Select NP_000917.3:n.-326_-325del
NM_001271162.1:c.-146+32_-146+33del (PGR) NP_001258091.1:n.-146+32_-146+33del
NR_073144.1:n.320_321del (PGR-AS1)
XM_006718858.2:c.-326_-325del (PGR) XP_006718921.1:n.-326_-325del
XM_011542869.1:c.-326_-325del (PGR) XP_011541171.1:n.-326_-325del
XR_947831.1:n.1247_1248del (PGR)
XM_006718858.3:c.-326_-325del (PGR) XP_006718921.1:n.-326_-325del
XM_011542869.2:c.-326_-325del (PGR) XP_011541171.1:n.-326_-325del
NM_001271162.2:c.-146+32_-146+33del (PGR) NP_001258091.1:n.-146+32_-146+33del
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