Canonical Allele Identifier: CA382436261

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922248C>A (hg19) ; chr11:g.101051517C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051517C>A , CM000673.2:g.101051517C>A	GRCh38
NC_000011.9:g.100922248C>A , CM000673.1:g.100922248C>A	GRCh37
NC_000011.8:g.100427458C>A	NCBI36
NG_016475.1:g.83297G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2264G>T MANE Select	ENSP00000325120.5:p.Trp755Leu
ENST00000263463.9:c.1958G>T	ENSP00000263463.5:p.Trp653Leu
ENST00000325455.9:c.2264G>T	ENSP00000325120.5:p.Trp755Leu
ENST00000526300.5:c.1958G>T	ENSP00000436803.1:p.Trp653Leu
ENST00000528960.5:c.2147G>T	ENSP00000432914.1:p.Trp716Leu
ENST00000533207.5:n.1631G>T
ENST00000534013.5:c.482G>T	ENSP00000436561.1:p.Trp161Leu
ENST00000534780.5:c.2264G>T	ENSP00000432352.1:p.Trp755Leu
ENST00000617858.4:c.1958G>T	ENSP00000481227.1:p.Trp653Leu
ENST00000619228.2:c.2147G>T	ENSP00000482698.1:p.Trp716Leu
NM_000926.4:c.2264G>T MANE Select	NP_000917.3:p.Trp755Leu
NM_001202474.3:c.1772G>T	NP_001189403.1:p.Trp591Leu
NM_001271161.2:c.1466G>T	NP_001258090.1:p.Trp489Leu
NM_001271162.1:c.482G>T	NP_001258091.1:p.Trp161Leu
NR_073141.2:n.2257G>T
NR_073142.2:n.2140G>T
NR_073143.2:n.1951G>T
XM_006718858.2:c.2264G>T	XP_006718921.1:p.Trp755Leu
XR_947831.1:n.3945G>T
XM_006718858.3:c.2264G>T	XP_006718921.1:p.Trp755Leu
NM_001271162.2:c.482G>T	NP_001258091.1:p.Trp161Leu
NR_073141.3:n.2271G>T
NR_073142.3:n.2154G>T
NR_073143.3:n.1965G>T