Canonical Allele Identifier: CA382436100

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922180A>C (hg19) ; chr11:g.101051449A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051449A>C , CM000673.2:g.101051449A>C	GRCh38
NC_000011.9:g.100922180A>C , CM000673.1:g.100922180A>C	GRCh37
NC_000011.8:g.100427390A>C	NCBI36
NG_016475.1:g.83365T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2332T>G MANE Select	ENSP00000325120.5:p.Phe778Val
ENST00000263463.9:c.2026T>G	ENSP00000263463.5:p.Phe676Val
ENST00000325455.9:c.2332T>G	ENSP00000325120.5:p.Phe778Val
ENST00000526300.5:c.2026T>G	ENSP00000436803.1:p.Phe676Val
ENST00000528960.5:c.2215T>G	ENSP00000432914.1:p.Phe739Val
ENST00000530764.1:n.22T>G
ENST00000533207.5:n.1699T>G
ENST00000534013.5:c.550T>G	ENSP00000436561.1:p.Phe184Val
ENST00000534780.5:c.2332T>G	ENSP00000432352.1:p.Phe778Val
ENST00000617858.4:c.2026T>G	ENSP00000481227.1:p.Phe676Val
ENST00000619228.2:c.2215T>G	ENSP00000482698.1:p.Phe739Val
NM_000926.4:c.2332T>G MANE Select	NP_000917.3:p.Phe778Val
NM_001202474.3:c.1840T>G	NP_001189403.1:p.Phe614Val
NM_001271161.2:c.1534T>G	NP_001258090.1:p.Phe512Val
NM_001271162.1:c.550T>G	NP_001258091.1:p.Phe184Val
NR_073141.2:n.2325T>G
NR_073142.2:n.2208T>G
NR_073143.2:n.2019T>G
XM_006718858.2:c.2332T>G	XP_006718921.1:p.Phe778Val
XM_006718858.3:c.2332T>G	XP_006718921.1:p.Phe778Val
NM_001271162.2:c.550T>G	NP_001258091.1:p.Phe184Val
NR_073141.3:n.2339T>G
NR_073142.3:n.2222T>G
NR_073143.3:n.2033T>G