Canonical Allele Identifier: CA382437212

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100933429A>G (hg19) ; chr11:g.101062698A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062698A>G , CM000673.2:g.101062698A>G	GRCh38
NC_000011.9:g.100933429A>G , CM000673.1:g.100933429A>G	GRCh37
NC_000011.8:g.100438639A>G	NCBI36
NG_016475.1:g.72116T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.1961T>C MANE Select	ENSP00000325120.5:p.Val654Ala
ENST00000263463.9:c.1907-11130T>C	ENSP00000263463.5:n.1907-11130T>C
ENST00000325455.9:c.1961T>C	ENSP00000325120.5:p.Val654Ala
ENST00000526300.5:c.1907-11130T>C	ENSP00000436803.1:n.1907-11130T>C
ENST00000528960.5:c.1844T>C	ENSP00000432914.1:p.Val615Ala
ENST00000533207.5:n.1328T>C
ENST00000534013.5:c.179T>C	ENSP00000436561.1:p.Val60Ala
ENST00000534780.5:c.1961T>C	ENSP00000432352.1:p.Val654Ala
ENST00000617858.4:c.1907-11130T>C	ENSP00000481227.1:n.1907-11130T>C
ENST00000619228.2:c.1844T>C	ENSP00000482698.1:p.Val615Ala
ENST00000632634.1:c.383T>C	ENSP00000487607.1:p.Val128Ala
NM_000926.4:c.1961T>C MANE Select	NP_000917.3:p.Val654Ala
NM_001202474.3:c.1469T>C	NP_001189403.1:p.Val490Ala
NM_001271161.2:c.1415-11130T>C	NP_001258090.1:n.1415-11130T>C
NM_001271162.1:c.179T>C	NP_001258091.1:p.Val60Ala
NR_073141.2:n.1954T>C
NR_073142.2:n.1837T>C
NR_073143.2:n.1900-11130T>C
XM_006718858.2:c.1961T>C	XP_006718921.1:p.Val654Ala
XR_947831.1:n.3533T>C
XM_006718858.3:c.1961T>C	XP_006718921.1:p.Val654Ala
NM_001271162.2:c.179T>C	NP_001258091.1:p.Val60Ala
NR_073141.3:n.1968T>C
NR_073142.3:n.1851T>C
NR_073143.3:n.1914-11130T>C