Canonical Allele Identifier: CA382436657

Gene: PGR

Linked Data

• COSMIC: COSM3687002 ; COSM4782648
• MyVariant Identifiers: chr11:g.100933233A>T (hg19) ; chr11:g.101062502A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062502A>T , CM000673.2:g.101062502A>T	GRCh38
NC_000011.9:g.100933233A>T , CM000673.1:g.100933233A>T	GRCh37
NC_000011.8:g.100438443A>T	NCBI36
NG_016475.1:g.72312T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2157T>A MANE Select	ENSP00000325120.5:p.Asn719Lys
ENST00000263463.9:c.1907-10934T>A	ENSP00000263463.5:n.1907-10934T>A
ENST00000325455.9:c.2157T>A	ENSP00000325120.5:p.Asn719Lys
ENST00000526300.5:c.1907-10934T>A	ENSP00000436803.1:n.1907-10934T>A
ENST00000528960.5:c.2040T>A	ENSP00000432914.1:p.Asn680Lys
ENST00000533207.5:n.1524T>A
ENST00000534013.5:c.375T>A	ENSP00000436561.1:p.Asn125Lys
ENST00000534780.5:c.2157T>A	ENSP00000432352.1:p.Asn719Lys
ENST00000617858.4:c.1907-10934T>A	ENSP00000481227.1:n.1907-10934T>A
ENST00000619228.2:c.2040T>A	ENSP00000482698.1:p.Asn680Lys
NM_000926.4:c.2157T>A MANE Select	NP_000917.3:p.Asn719Lys
NM_001202474.3:c.1665T>A	NP_001189403.1:p.Asn555Lys
NM_001271161.2:c.1415-10934T>A	NP_001258090.1:n.1415-10934T>A
NM_001271162.1:c.375T>A	NP_001258091.1:p.Asn125Lys
NR_073141.2:n.2150T>A
NR_073142.2:n.2033T>A
NR_073143.2:n.1900-10934T>A
XM_006718858.2:c.2157T>A	XP_006718921.1:p.Asn719Lys
XR_947831.1:n.3729T>A
XM_006718858.3:c.2157T>A	XP_006718921.1:p.Asn719Lys
NM_001271162.2:c.375T>A	NP_001258091.1:p.Asn125Lys
NR_073141.3:n.2164T>A
NR_073142.3:n.2047T>A
NR_073143.3:n.1914-10934T>A