Canonical Allele Identifier: CA382436834

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100933313T>A (hg19) ; chr11:g.101062582T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062582T>A , CM000673.2:g.101062582T>A	GRCh38
NC_000011.9:g.100933313T>A , CM000673.1:g.100933313T>A	GRCh37
NC_000011.8:g.100438523T>A	NCBI36
NG_016475.1:g.72232A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.2077A>T MANE Select	ENSP00000325120.5:p.Ser693Cys
ENST00000263463.9:c.1907-11014A>T	ENSP00000263463.5:n.1907-11014A>T
ENST00000325455.9:c.2077A>T	ENSP00000325120.5:p.Ser693Cys
ENST00000526300.5:c.1907-11014A>T	ENSP00000436803.1:n.1907-11014A>T
ENST00000528960.5:c.1960A>T	ENSP00000432914.1:p.Ser654Cys
ENST00000533207.5:n.1444A>T
ENST00000534013.5:c.295A>T	ENSP00000436561.1:p.Ser99Cys
ENST00000534780.5:c.2077A>T	ENSP00000432352.1:p.Ser693Cys
ENST00000617858.4:c.1907-11014A>T	ENSP00000481227.1:n.1907-11014A>T
ENST00000619228.2:c.1960A>T	ENSP00000482698.1:p.Ser654Cys
ENST00000632634.1:c.499A>T	ENSP00000487607.1:p.Ser167Cys
NM_000926.4:c.2077A>T MANE Select	NP_000917.3:p.Ser693Cys
NM_001202474.3:c.1585A>T	NP_001189403.1:p.Ser529Cys
NM_001271161.2:c.1415-11014A>T	NP_001258090.1:n.1415-11014A>T
NM_001271162.1:c.295A>T	NP_001258091.1:p.Ser99Cys
NR_073141.2:n.2070A>T
NR_073142.2:n.1953A>T
NR_073143.2:n.1900-11014A>T
XM_006718858.2:c.2077A>T	XP_006718921.1:p.Ser693Cys
XR_947831.1:n.3649A>T
XM_006718858.3:c.2077A>T	XP_006718921.1:p.Ser693Cys
NM_001271162.2:c.295A>T	NP_001258091.1:p.Ser99Cys
NR_073141.3:n.2084A>T
NR_073142.3:n.1967A>T
NR_073143.3:n.1914-11014A>T