Canonical Allele Identifier: CA382436369

Gene: PGR

Linked Data

• dbSNP Id: rs1315135533
• gnomAD v2: 11-100922294-G-A
• gnomAD v4: 11-101051563-G-A
• COSMIC: COSM1561169 ; COSM4424213
• MyVariant Identifiers: chr11:g.100922294G>A (hg19) ; chr11:g.101051563G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051563G>A , CM000673.2:g.101051563G>A	GRCh38
NC_000011.9:g.100922294G>A , CM000673.1:g.100922294G>A	GRCh37
NC_000011.8:g.100427504G>A	NCBI36
NG_016475.1:g.83251C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2218C>T MANE Select	ENSP00000325120.5:p.Arg740Ter
ENST00000263463.9:c.1912C>T	ENSP00000263463.5:p.Arg638Ter
ENST00000325455.9:c.2218C>T	ENSP00000325120.5:p.Arg740Ter
ENST00000526300.5:c.1912C>T	ENSP00000436803.1:p.Arg638Ter
ENST00000528960.5:c.2101C>T	ENSP00000432914.1:p.Arg701Ter
ENST00000533207.5:n.1585C>T
ENST00000534013.5:c.436C>T	ENSP00000436561.1:p.Arg146Ter
ENST00000534780.5:c.2218C>T	ENSP00000432352.1:p.Arg740Ter
ENST00000617858.4:c.1912C>T	ENSP00000481227.1:p.Arg638Ter
ENST00000619228.2:c.2101C>T	ENSP00000482698.1:p.Arg701Ter
NM_000926.4:c.2218C>T MANE Select	NP_000917.3:p.Arg740Ter
NM_001202474.3:c.1726C>T	NP_001189403.1:p.Arg576Ter
NM_001271161.2:c.1420C>T	NP_001258090.1:p.Arg474Ter
NM_001271162.1:c.436C>T	NP_001258091.1:p.Arg146Ter
NR_073141.2:n.2211C>T
NR_073142.2:n.2094C>T
NR_073143.2:n.1905C>T
XM_006718858.2:c.2218C>T	XP_006718921.1:p.Arg740Ter
XR_947831.1:n.3899C>T
XM_006718858.3:c.2218C>T	XP_006718921.1:p.Arg740Ter
NM_001271162.2:c.436C>T	NP_001258091.1:p.Arg146Ter
NR_073141.3:n.2225C>T
NR_073142.3:n.2108C>T
NR_073143.3:n.1919C>T