Canonical Allele Identifier: CA1995637118
Gene: PGR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101034472G= , CM000673.2:g.101034472G= GRCh38
NC_000011.9:g.100905203G= , CM000673.1:g.100905203G= GRCh37
NC_000011.8:g.100410413G= NCBI36
NG_016475.1:g.100342C=

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.*4644C= MANE Select ENSP00000325120.5:n.*4644C=
ENST00000325455.9:c.*4644C= ENSP00000325120.5:n.*4644C=
NM_000926.4:c.*4644C= MANE Select NP_000917.3:n.*4644C=
NM_001202474.3:c.*4644C= NP_001189403.1:n.*4644C=
NM_001271161.2:c.*4644C= NP_001258090.1:n.*4644C=
NM_001271162.1:c.*4644C= NP_001258091.1:n.*4644C=
NR_073141.2:n.7387C=
NR_073142.2:n.7270C=
NR_073143.2:n.7002C=
NM_001271162.2:c.*4644C= NP_001258091.1:n.*4644C=
NR_073141.3:n.7401C=
NR_073142.3:n.7284C=
NR_073143.3:n.7016C=