Canonical Allele Identifier: CA382436926

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100933348A>G (hg19) ; chr11:g.101062617A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062617A>G , CM000673.2:g.101062617A>G	GRCh38
NC_000011.9:g.100933348A>G , CM000673.1:g.100933348A>G	GRCh37
NC_000011.8:g.100438558A>G	NCBI36
NG_016475.1:g.72197T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2042T>C MANE Select	ENSP00000325120.5:p.Ile681Thr
ENST00000263463.9:c.1907-11049T>C	ENSP00000263463.5:n.1907-11049T>C
ENST00000325455.9:c.2042T>C	ENSP00000325120.5:p.Ile681Thr
ENST00000526300.5:c.1907-11049T>C	ENSP00000436803.1:n.1907-11049T>C
ENST00000528960.5:c.1925T>C	ENSP00000432914.1:p.Ile642Thr
ENST00000533207.5:n.1409T>C
ENST00000534013.5:c.260T>C	ENSP00000436561.1:p.Ile87Thr
ENST00000534780.5:c.2042T>C	ENSP00000432352.1:p.Ile681Thr
ENST00000617858.4:c.1907-11049T>C	ENSP00000481227.1:n.1907-11049T>C
ENST00000619228.2:c.1925T>C	ENSP00000482698.1:p.Ile642Thr
ENST00000632634.1:c.464T>C	ENSP00000487607.1:p.Ile155Thr
NM_000926.4:c.2042T>C MANE Select	NP_000917.3:p.Ile681Thr
NM_001202474.3:c.1550T>C	NP_001189403.1:p.Ile517Thr
NM_001271161.2:c.1415-11049T>C	NP_001258090.1:n.1415-11049T>C
NM_001271162.1:c.260T>C	NP_001258091.1:p.Ile87Thr
NR_073141.2:n.2035T>C
NR_073142.2:n.1918T>C
NR_073143.2:n.1900-11049T>C
XM_006718858.2:c.2042T>C	XP_006718921.1:p.Ile681Thr
XR_947831.1:n.3614T>C
XM_006718858.3:c.2042T>C	XP_006718921.1:p.Ile681Thr
NM_001271162.2:c.260T>C	NP_001258091.1:p.Ile87Thr
NR_073141.3:n.2049T>C
NR_073142.3:n.1932T>C
NR_073143.3:n.1914-11049T>C