Canonical Allele Identifier: CA670697191

Gene: PGR

Linked Data

• dbSNP Id: rs1416404838
• gnomAD v3: 11-101034800-G-A
• gnomAD v4: 11-101034800-G-A
• MyVariant Identifiers: chr11:g.100905531G>A (hg19) ; chr11:g.101034800G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034800G>A , CM000673.2:g.101034800G>A	GRCh38
NC_000011.9:g.100905531G>A , CM000673.1:g.100905531G>A	GRCh37
NC_000011.8:g.100410741G>A	NCBI36
NG_016475.1:g.100014C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4316C>T MANE Select	ENSP00000325120.5:n.*4316C>T
ENST00000325455.9:c.*4316C>T	ENSP00000325120.5:n.*4316C>T
NM_000926.4:c.*4316C>T MANE Select	NP_000917.3:n.*4316C>T
NM_001202474.3:c.*4316C>T	NP_001189403.1:n.*4316C>T
NM_001271161.2:c.*4316C>T	NP_001258090.1:n.*4316C>T
NM_001271162.1:c.*4316C>T	NP_001258091.1:n.*4316C>T
NR_073141.2:n.7059C>T
NR_073142.2:n.6942C>T
NR_073143.2:n.6674C>T
NM_001271162.2:c.*4316C>T	NP_001258091.1:n.*4316C>T
NR_073141.3:n.7073C>T
NR_073142.3:n.6956C>T
NR_073143.3:n.6688C>T