Canonical Allele Identifier: CA1995637095

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034391_101034394delinsAAGG , CM000673.2:g.101034391_101034394delinsAAGG	GRCh38
NC_000011.9:g.100905122_100905125delinsAAGG , CM000673.1:g.100905122_100905125delinsAAGG	GRCh37
NC_000011.8:g.100410332_100410335delinsAAGG	NCBI36
NG_016475.1:g.100420_100423delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4722_*4725delinsCCTT MANE Select	ENSP00000325120.5:n.*4722_*4725delinsCCTT
ENST00000325455.9:c.*4722_*4725delinsCCTT	ENSP00000325120.5:n.*4722_*4725delinsCCTT
NM_000926.4:c.*4722_*4725delinsCCTT MANE Select	NP_000917.3:n.*4722_*4725delinsCCTT
NM_001202474.3:c.*4722_*4725delinsCCTT	NP_001189403.1:n.*4722_*4725delinsCCTT
NM_001271161.2:c.*4722_*4725delinsCCTT	NP_001258090.1:n.*4722_*4725delinsCCTT
NM_001271162.1:c.*4722_*4725delinsCCTT	NP_001258091.1:n.*4722_*4725delinsCCTT
NR_073141.2:n.7465_7468delinsCCTT
NR_073142.2:n.7348_7351delinsCCTT
NR_073143.2:n.7080_7083delinsCCTT
NM_001271162.2:c.*4722_*4725delinsCCTT	NP_001258091.1:n.*4722_*4725delinsCCTT
NR_073141.3:n.7479_7482delinsCCTT
NR_073142.3:n.7362_7365delinsCCTT
NR_073143.3:n.7094_7097delinsCCTT