Canonical Allele Identifier: CA670697200

Gene: PGR

Linked Data

• dbSNP Id: rs1369771916
• gnomAD v3: 11-101034831-A-T
• gnomAD v4: 11-101034831-A-T
• MyVariant Identifiers: chr11:g.100905562A>T (hg19) ; chr11:g.101034831A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034831A>T , CM000673.2:g.101034831A>T	GRCh38
NC_000011.9:g.100905562A>T , CM000673.1:g.100905562A>T	GRCh37
NC_000011.8:g.100410772A>T	NCBI36
NG_016475.1:g.99983T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4285T>A MANE Select	ENSP00000325120.5:n.*4285T>A
ENST00000325455.9:c.*4285T>A	ENSP00000325120.5:n.*4285T>A
NM_000926.4:c.*4285T>A MANE Select	NP_000917.3:n.*4285T>A
NM_001202474.3:c.*4285T>A	NP_001189403.1:n.*4285T>A
NM_001271161.2:c.*4285T>A	NP_001258090.1:n.*4285T>A
NM_001271162.1:c.*4285T>A	NP_001258091.1:n.*4285T>A
NR_073141.2:n.7028T>A
NR_073142.2:n.6911T>A
NR_073143.2:n.6643T>A
NM_001271162.2:c.*4285T>A	NP_001258091.1:n.*4285T>A
NR_073141.3:n.7042T>A
NR_073142.3:n.6925T>A
NR_073143.3:n.6657T>A