Canonical Allele Identifier: CA382436846

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100933318A>C (hg19) ; chr11:g.101062587A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062587A>C , CM000673.2:g.101062587A>C	GRCh38
NC_000011.9:g.100933318A>C , CM000673.1:g.100933318A>C	GRCh37
NC_000011.8:g.100438528A>C	NCBI36
NG_016475.1:g.72227T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2072T>G MANE Select	ENSP00000325120.5:p.Leu691Ter
ENST00000263463.9:c.1907-11019T>G	ENSP00000263463.5:n.1907-11019T>G
ENST00000325455.9:c.2072T>G	ENSP00000325120.5:p.Leu691Ter
ENST00000526300.5:c.1907-11019T>G	ENSP00000436803.1:n.1907-11019T>G
ENST00000528960.5:c.1955T>G	ENSP00000432914.1:p.Leu652Ter
ENST00000533207.5:n.1439T>G
ENST00000534013.5:c.290T>G	ENSP00000436561.1:p.Leu97Ter
ENST00000534780.5:c.2072T>G	ENSP00000432352.1:p.Leu691Ter
ENST00000617858.4:c.1907-11019T>G	ENSP00000481227.1:n.1907-11019T>G
ENST00000619228.2:c.1955T>G	ENSP00000482698.1:p.Leu652Ter
ENST00000632634.1:c.494T>G	ENSP00000487607.1:p.Leu165Ter
NM_000926.4:c.2072T>G MANE Select	NP_000917.3:p.Leu691Ter
NM_001202474.3:c.1580T>G	NP_001189403.1:p.Leu527Ter
NM_001271161.2:c.1415-11019T>G	NP_001258090.1:n.1415-11019T>G
NM_001271162.1:c.290T>G	NP_001258091.1:p.Leu97Ter
NR_073141.2:n.2065T>G
NR_073142.2:n.1948T>G
NR_073143.2:n.1900-11019T>G
XM_006718858.2:c.2072T>G	XP_006718921.1:p.Leu691Ter
XR_947831.1:n.3644T>G
XM_006718858.3:c.2072T>G	XP_006718921.1:p.Leu691Ter
NM_001271162.2:c.290T>G	NP_001258091.1:p.Leu97Ter
NR_073141.3:n.2079T>G
NR_073142.3:n.1962T>G
NR_073143.3:n.1914-11019T>G