Canonical Allele Identifier: CA382436313

Gene: PGR

Linked Data

• dbSNP Id: rs1458837648
• gnomAD v2: 11-100922270-T-C
• gnomAD v4: 11-101051539-T-C
• MyVariant Identifiers: chr11:g.100922270T>C (hg19) ; chr11:g.101051539T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051539T>C , CM000673.2:g.101051539T>C	GRCh38
NC_000011.9:g.100922270T>C , CM000673.1:g.100922270T>C	GRCh37
NC_000011.8:g.100427480T>C	NCBI36
NG_016475.1:g.83275A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2242A>G MANE Select	ENSP00000325120.5:p.Ile748Val
ENST00000263463.9:c.1936A>G	ENSP00000263463.5:p.Ile646Val
ENST00000325455.9:c.2242A>G	ENSP00000325120.5:p.Ile748Val
ENST00000526300.5:c.1936A>G	ENSP00000436803.1:p.Ile646Val
ENST00000528960.5:c.2125A>G	ENSP00000432914.1:p.Ile709Val
ENST00000533207.5:n.1609A>G
ENST00000534013.5:c.460A>G	ENSP00000436561.1:p.Ile154Val
ENST00000534780.5:c.2242A>G	ENSP00000432352.1:p.Ile748Val
ENST00000617858.4:c.1936A>G	ENSP00000481227.1:p.Ile646Val
ENST00000619228.2:c.2125A>G	ENSP00000482698.1:p.Ile709Val
NM_000926.4:c.2242A>G MANE Select	NP_000917.3:p.Ile748Val
NM_001202474.3:c.1750A>G	NP_001189403.1:p.Ile584Val
NM_001271161.2:c.1444A>G	NP_001258090.1:p.Ile482Val
NM_001271162.1:c.460A>G	NP_001258091.1:p.Ile154Val
NR_073141.2:n.2235A>G
NR_073142.2:n.2118A>G
NR_073143.2:n.1929A>G
XM_006718858.2:c.2242A>G	XP_006718921.1:p.Ile748Val
XR_947831.1:n.3923A>G
XM_006718858.3:c.2242A>G	XP_006718921.1:p.Ile748Val
NM_001271162.2:c.460A>G	NP_001258091.1:p.Ile154Val
NR_073141.3:n.2249A>G
NR_073142.3:n.2132A>G
NR_073143.3:n.1943A>G