Canonical Allele Identifier: CA382437194

Gene: PGR

Linked Data

• dbSNP Id: rs1591381326
• MyVariant Identifiers: chr11:g.100933423A>G (hg19) ; chr11:g.101062692A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062692A>G , CM000673.2:g.101062692A>G	GRCh38
NC_000011.9:g.100933423A>G , CM000673.1:g.100933423A>G	GRCh37
NC_000011.8:g.100438633A>G	NCBI36
NG_016475.1:g.72122T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.1967T>C MANE Select	ENSP00000325120.5:p.Leu656Pro
ENST00000263463.9:c.1907-11124T>C	ENSP00000263463.5:n.1907-11124T>C
ENST00000325455.9:c.1967T>C	ENSP00000325120.5:p.Leu656Pro
ENST00000526300.5:c.1907-11124T>C	ENSP00000436803.1:n.1907-11124T>C
ENST00000528960.5:c.1850T>C	ENSP00000432914.1:p.Leu617Pro
ENST00000533207.5:n.1334T>C
ENST00000534013.5:c.185T>C	ENSP00000436561.1:p.Leu62Pro
ENST00000534780.5:c.1967T>C	ENSP00000432352.1:p.Leu656Pro
ENST00000617858.4:c.1907-11124T>C	ENSP00000481227.1:n.1907-11124T>C
ENST00000619228.2:c.1850T>C	ENSP00000482698.1:p.Leu617Pro
ENST00000632634.1:c.389T>C	ENSP00000487607.1:p.Leu130Pro
NM_000926.4:c.1967T>C MANE Select	NP_000917.3:p.Leu656Pro
NM_001202474.3:c.1475T>C	NP_001189403.1:p.Leu492Pro
NM_001271161.2:c.1415-11124T>C	NP_001258090.1:n.1415-11124T>C
NM_001271162.1:c.185T>C	NP_001258091.1:p.Leu62Pro
NR_073141.2:n.1960T>C
NR_073142.2:n.1843T>C
NR_073143.2:n.1900-11124T>C
XM_006718858.2:c.1967T>C	XP_006718921.1:p.Leu656Pro
XR_947831.1:n.3539T>C
XM_006718858.3:c.1967T>C	XP_006718921.1:p.Leu656Pro
NM_001271162.2:c.185T>C	NP_001258091.1:p.Leu62Pro
NR_073141.3:n.1974T>C
NR_073142.3:n.1857T>C
NR_073143.3:n.1914-11124T>C