Canonical Allele Identifier: CA382436130

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922192G>C (hg19) ; chr11:g.101051461G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051461G>C , CM000673.2:g.101051461G>C	GRCh38
NC_000011.9:g.100922192G>C , CM000673.1:g.100922192G>C	GRCh37
NC_000011.8:g.100427402G>C	NCBI36
NG_016475.1:g.83353C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2320C>G MANE Select	ENSP00000325120.5:p.Gln774Glu
ENST00000263463.9:c.2014C>G	ENSP00000263463.5:p.Gln672Glu
ENST00000325455.9:c.2320C>G	ENSP00000325120.5:p.Gln774Glu
ENST00000526300.5:c.2014C>G	ENSP00000436803.1:p.Gln672Glu
ENST00000528960.5:c.2203C>G	ENSP00000432914.1:p.Gln735Glu
ENST00000530764.1:n.10C>G
ENST00000533207.5:n.1687C>G
ENST00000534013.5:c.538C>G	ENSP00000436561.1:p.Gln180Glu
ENST00000534780.5:c.2320C>G	ENSP00000432352.1:p.Gln774Glu
ENST00000617858.4:c.2014C>G	ENSP00000481227.1:p.Gln672Glu
ENST00000619228.2:c.2203C>G	ENSP00000482698.1:p.Gln735Glu
NM_000926.4:c.2320C>G MANE Select	NP_000917.3:p.Gln774Glu
NM_001202474.3:c.1828C>G	NP_001189403.1:p.Gln610Glu
NM_001271161.2:c.1522C>G	NP_001258090.1:p.Gln508Glu
NM_001271162.1:c.538C>G	NP_001258091.1:p.Gln180Glu
NR_073141.2:n.2313C>G
NR_073142.2:n.2196C>G
NR_073143.2:n.2007C>G
XM_006718858.2:c.2320C>G	XP_006718921.1:p.Gln774Glu
XM_006718858.3:c.2320C>G	XP_006718921.1:p.Gln774Glu
NM_001271162.2:c.538C>G	NP_001258091.1:p.Gln180Glu
NR_073141.3:n.2327C>G
NR_073142.3:n.2210C>G
NR_073143.3:n.2021C>G