Canonical Allele Identifier: CA476545426

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100933416C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062685C>T , CM000673.2:g.101062685C>T	GRCh38
NC_000011.9:g.100933416C>T , CM000673.1:g.100933416C>T	GRCh37
NC_000011.8:g.100438626C>T	NCBI36
NG_016475.1:g.72129G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.1974G>A MANE Select	ENSP00000325120.5:p.Gln658=
ENST00000263463.9:c.1907-11117G>A	ENSP00000263463.5:n.1907-11117G>A
ENST00000325455.9:c.1974G>A	ENSP00000325120.5:p.Gln658=
ENST00000526300.5:c.1907-11117G>A	ENSP00000436803.1:n.1907-11117G>A
ENST00000528960.5:c.1857G>A	ENSP00000432914.1:p.Gln619=
ENST00000533207.5:n.1341G>A
ENST00000534013.5:c.192G>A	ENSP00000436561.1:p.Gln64=
ENST00000534780.5:c.1974G>A	ENSP00000432352.1:p.Gln658=
ENST00000617858.4:c.1907-11117G>A	ENSP00000481227.1:n.1907-11117G>A
ENST00000619228.2:c.1857G>A	ENSP00000482698.1:p.Gln619=
ENST00000632634.1:c.396G>A	ENSP00000487607.1:p.Gln132=
NM_000926.4:c.1974G>A MANE Select	NP_000917.3:p.Gln658=
NM_001202474.3:c.1482G>A	NP_001189403.1:p.Gln494=
NM_001271161.2:c.1415-11117G>A	NP_001258090.1:n.1415-11117G>A
NM_001271162.1:c.192G>A	NP_001258091.1:p.Gln64=
NR_073141.2:n.1967G>A
NR_073142.2:n.1850G>A
NR_073143.2:n.1900-11117G>A
XM_006718858.2:c.1974G>A	XP_006718921.1:p.Gln658=
XR_947831.1:n.3546G>A
XM_006718858.3:c.1974G>A	XP_006718921.1:p.Gln658=
NM_001271162.2:c.192G>A	NP_001258091.1:p.Gln64=
NR_073141.3:n.1981G>A
NR_073142.3:n.1864G>A
NR_073143.3:n.1914-11117G>A