Canonical Allele Identifier: CA476501637

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922271C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051540C>T , CM000673.2:g.101051540C>T	GRCh38
NC_000011.9:g.100922271C>T , CM000673.1:g.100922271C>T	GRCh37
NC_000011.8:g.100427481C>T	NCBI36
NG_016475.1:g.83274G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2241G>A MANE Select	ENSP00000325120.5:p.Gln747=
ENST00000263463.9:c.1935G>A	ENSP00000263463.5:p.Gln645=
ENST00000325455.9:c.2241G>A	ENSP00000325120.5:p.Gln747=
ENST00000526300.5:c.1935G>A	ENSP00000436803.1:p.Gln645=
ENST00000528960.5:c.2124G>A	ENSP00000432914.1:p.Gln708=
ENST00000533207.5:n.1608G>A
ENST00000534013.5:c.459G>A	ENSP00000436561.1:p.Gln153=
ENST00000534780.5:c.2241G>A	ENSP00000432352.1:p.Gln747=
ENST00000617858.4:c.1935G>A	ENSP00000481227.1:p.Gln645=
ENST00000619228.2:c.2124G>A	ENSP00000482698.1:p.Gln708=
NM_000926.4:c.2241G>A MANE Select	NP_000917.3:p.Gln747=
NM_001202474.3:c.1749G>A	NP_001189403.1:p.Gln583=
NM_001271161.2:c.1443G>A	NP_001258090.1:p.Gln481=
NM_001271162.1:c.459G>A	NP_001258091.1:p.Gln153=
NR_073141.2:n.2234G>A
NR_073142.2:n.2117G>A
NR_073143.2:n.1928G>A
XM_006718858.2:c.2241G>A	XP_006718921.1:p.Gln747=
XR_947831.1:n.3922G>A
XM_006718858.3:c.2241G>A	XP_006718921.1:p.Gln747=
NM_001271162.2:c.459G>A	NP_001258091.1:p.Gln153=
NR_073141.3:n.2248G>A
NR_073142.3:n.2131G>A
NR_073143.3:n.1942G>A