Canonical Allele Identifier: CA1995637234

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034729_101034732delinsGCCC , CM000673.2:g.101034729_101034732delinsGCCC	GRCh38
NC_000011.9:g.100905460_100905463delinsGCCC , CM000673.1:g.100905460_100905463delinsGCCC	GRCh37
NC_000011.8:g.100410670_100410673delinsGCCC	NCBI36
NG_016475.1:g.100082_100085delinsGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4384_*4387delinsGGGC MANE Select	ENSP00000325120.5:n.*4384_*4387delinsGGGC
ENST00000325455.9:c.*4384_*4387delinsGGGC	ENSP00000325120.5:n.*4384_*4387delinsGGGC
NM_000926.4:c.*4384_*4387delinsGGGC MANE Select	NP_000917.3:n.*4384_*4387delinsGGGC
NM_001202474.3:c.*4384_*4387delinsGGGC	NP_001189403.1:n.*4384_*4387delinsGGGC
NM_001271161.2:c.*4384_*4387delinsGGGC	NP_001258090.1:n.*4384_*4387delinsGGGC
NM_001271162.1:c.*4384_*4387delinsGGGC	NP_001258091.1:n.*4384_*4387delinsGGGC
NR_073141.2:n.7127_7130delinsGGGC
NR_073142.2:n.7010_7013delinsGGGC
NR_073143.2:n.6742_6745delinsGGGC
NM_001271162.2:c.*4384_*4387delinsGGGC	NP_001258091.1:n.*4384_*4387delinsGGGC
NR_073141.3:n.7141_7144delinsGGGC
NR_073142.3:n.7024_7027delinsGGGC
NR_073143.3:n.6756_6759delinsGGGC