Canonical Allele Identifier: CA382436981

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100933363G>C (hg19) ; chr11:g.101062632G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062632G>C , CM000673.2:g.101062632G>C	GRCh38
NC_000011.9:g.100933363G>C , CM000673.1:g.100933363G>C	GRCh37
NC_000011.8:g.100438573G>C	NCBI36
NG_016475.1:g.72182C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2027C>G MANE Select	ENSP00000325120.5:p.Ser676Ter
ENST00000263463.9:c.1907-11064C>G	ENSP00000263463.5:n.1907-11064C>G
ENST00000325455.9:c.2027C>G	ENSP00000325120.5:p.Ser676Ter
ENST00000526300.5:c.1907-11064C>G	ENSP00000436803.1:n.1907-11064C>G
ENST00000528960.5:c.1910C>G	ENSP00000432914.1:p.Ser637Ter
ENST00000533207.5:n.1394C>G
ENST00000534013.5:c.245C>G	ENSP00000436561.1:p.Ser82Ter
ENST00000534780.5:c.2027C>G	ENSP00000432352.1:p.Ser676Ter
ENST00000617858.4:c.1907-11064C>G	ENSP00000481227.1:n.1907-11064C>G
ENST00000619228.2:c.1910C>G	ENSP00000482698.1:p.Ser637Ter
ENST00000632634.1:c.449C>G	ENSP00000487607.1:p.Ser150Ter
NM_000926.4:c.2027C>G MANE Select	NP_000917.3:p.Ser676Ter
NM_001202474.3:c.1535C>G	NP_001189403.1:p.Ser512Ter
NM_001271161.2:c.1415-11064C>G	NP_001258090.1:n.1415-11064C>G
NM_001271162.1:c.245C>G	NP_001258091.1:p.Ser82Ter
NR_073141.2:n.2020C>G
NR_073142.2:n.1903C>G
NR_073143.2:n.1900-11064C>G
XM_006718858.2:c.2027C>G	XP_006718921.1:p.Ser676Ter
XR_947831.1:n.3599C>G
XM_006718858.3:c.2027C>G	XP_006718921.1:p.Ser676Ter
NM_001271162.2:c.245C>G	NP_001258091.1:p.Ser82Ter
NR_073141.3:n.2034C>G
NR_073142.3:n.1917C>G
NR_073143.3:n.1914-11064C>G