Canonical Allele Identifier: CA1995637160
Gene: PGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101034579T= , CM000673.2:g.101034579T= GRCh38
NC_000011.9:g.100905310T= , CM000673.1:g.100905310T= GRCh37
NC_000011.8:g.100410520T= NCBI36
NG_016475.1:g.100235A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000325455.10:c.*4537A= MANE Select ENSP00000325120.5:n.*4537A=
ENST00000325455.9:c.*4537A= ENSP00000325120.5:n.*4537A=
NM_000926.4:c.*4537A= MANE Select NP_000917.3:n.*4537A=
NM_001202474.3:c.*4537A= NP_001189403.1:n.*4537A=
NM_001271161.2:c.*4537A= NP_001258090.1:n.*4537A=
NM_001271162.1:c.*4537A= NP_001258091.1:n.*4537A=
NR_073141.2:n.7280A=
NR_073142.2:n.7163A=
NR_073143.2:n.6895A=
NM_001271162.2:c.*4537A= NP_001258091.1:n.*4537A=
NR_073141.3:n.7294A=
NR_073142.3:n.7177A=
NR_073143.3:n.6909A=