Canonical Allele Identifier: CA1995637228

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034718_101034724delinsCAATAAT , CM000673.2:g.101034718_101034724delinsCAATAAT	GRCh38
NC_000011.9:g.100905449_100905455delinsCAATAAT , CM000673.1:g.100905449_100905455delinsCAATAAT	GRCh37
NC_000011.8:g.100410659_100410665delinsCAATAAT	NCBI36
NG_016475.1:g.100090_100096delinsATTATTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4392_*4398delinsATTATTG MANE Select	ENSP00000325120.5:n.*4392_*4398delinsATTATTG
ENST00000325455.9:c.*4392_*4398delinsATTATTG	ENSP00000325120.5:n.*4392_*4398delinsATTATTG
NM_000926.4:c.*4392_*4398delinsATTATTG MANE Select	NP_000917.3:n.*4392_*4398delinsATTATTG
NM_001202474.3:c.*4392_*4398delinsATTATTG	NP_001189403.1:n.*4392_*4398delinsATTATTG
NM_001271161.2:c.*4392_*4398delinsATTATTG	NP_001258090.1:n.*4392_*4398delinsATTATTG
NM_001271162.1:c.*4392_*4398delinsATTATTG	NP_001258091.1:n.*4392_*4398delinsATTATTG
NR_073141.2:n.7135_7141delinsATTATTG
NR_073142.2:n.7018_7024delinsATTATTG
NR_073143.2:n.6750_6756delinsATTATTG
NM_001271162.2:c.*4392_*4398delinsATTATTG	NP_001258091.1:n.*4392_*4398delinsATTATTG
NR_073141.3:n.7149_7155delinsATTATTG
NR_073142.3:n.7032_7038delinsATTATTG
NR_073143.3:n.6764_6770delinsATTATTG