Canonical Allele Identifier: CA382436877

Gene: PGR

Linked Data

• dbSNP Id: rs1860543294
• gnomAD v4: 11-101062603-G-A
• COSMIC: COSM3985849 ; COSM4908560
• MyVariant Identifiers: chr11:g.100933334G>A (hg19) ; chr11:g.101062603G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062603G>A , CM000673.2:g.101062603G>A	GRCh38
NC_000011.9:g.100933334G>A , CM000673.1:g.100933334G>A	GRCh37
NC_000011.8:g.100438544G>A	NCBI36
NG_016475.1:g.72211C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2056C>T MANE Select	ENSP00000325120.5:p.Pro686Ser
ENST00000263463.9:c.1907-11035C>T	ENSP00000263463.5:n.1907-11035C>T
ENST00000325455.9:c.2056C>T	ENSP00000325120.5:p.Pro686Ser
ENST00000526300.5:c.1907-11035C>T	ENSP00000436803.1:n.1907-11035C>T
ENST00000528960.5:c.1939C>T	ENSP00000432914.1:p.Pro647Ser
ENST00000533207.5:n.1423C>T
ENST00000534013.5:c.274C>T	ENSP00000436561.1:p.Pro92Ser
ENST00000534780.5:c.2056C>T	ENSP00000432352.1:p.Pro686Ser
ENST00000617858.4:c.1907-11035C>T	ENSP00000481227.1:n.1907-11035C>T
ENST00000619228.2:c.1939C>T	ENSP00000482698.1:p.Pro647Ser
ENST00000632634.1:c.478C>T	ENSP00000487607.1:p.Pro160Ser
NM_000926.4:c.2056C>T MANE Select	NP_000917.3:p.Pro686Ser
NM_001202474.3:c.1564C>T	NP_001189403.1:p.Pro522Ser
NM_001271161.2:c.1415-11035C>T	NP_001258090.1:n.1415-11035C>T
NM_001271162.1:c.274C>T	NP_001258091.1:p.Pro92Ser
NR_073141.2:n.2049C>T
NR_073142.2:n.1932C>T
NR_073143.2:n.1900-11035C>T
XM_006718858.2:c.2056C>T	XP_006718921.1:p.Pro686Ser
XR_947831.1:n.3628C>T
XM_006718858.3:c.2056C>T	XP_006718921.1:p.Pro686Ser
NM_001271162.2:c.274C>T	NP_001258091.1:p.Pro92Ser
NR_073141.3:n.2063C>T
NR_073142.3:n.1946C>T
NR_073143.3:n.1914-11035C>T