Canonical Allele Identifier: CA2615658480

Gene: PGR

Linked Data

• gnomAD v4: 11-101034712-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034712T>A , CM000673.2:g.101034712T>A	GRCh38
NC_000011.9:g.100905443T>A , CM000673.1:g.100905443T>A	GRCh37
NC_000011.8:g.100410653T>A	NCBI36
NG_016475.1:g.100102A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4404A>T MANE Select	ENSP00000325120.5:n.*4404A>T
ENST00000325455.9:c.*4404A>T	ENSP00000325120.5:n.*4404A>T
NM_000926.4:c.*4404A>T MANE Select	NP_000917.3:n.*4404A>T
NM_001202474.3:c.*4404A>T	NP_001189403.1:n.*4404A>T
NM_001271161.2:c.*4404A>T	NP_001258090.1:n.*4404A>T
NM_001271162.1:c.*4404A>T	NP_001258091.1:n.*4404A>T
NR_073141.2:n.7147A>T
NR_073142.2:n.7030A>T
NR_073143.2:n.6762A>T
NM_001271162.2:c.*4404A>T	NP_001258091.1:n.*4404A>T
NR_073141.3:n.7161A>T
NR_073142.3:n.7044A>T
NR_073143.3:n.6776A>T