Canonical Allele Identifier: CA382436055

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922158T>G (hg19) ; chr11:g.101051427T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051427T>G , CM000673.2:g.101051427T>G	GRCh38
NC_000011.9:g.100922158T>G , CM000673.1:g.100922158T>G	GRCh37
NC_000011.8:g.100427368T>G	NCBI36
NG_016475.1:g.83387A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.2354A>C MANE Select	ENSP00000325120.5:p.Asn785Thr
ENST00000263463.9:c.2048A>C	ENSP00000263463.5:p.Asn683Thr
ENST00000325455.9:c.2354A>C	ENSP00000325120.5:p.Asn785Thr
ENST00000526300.5:c.2048A>C	ENSP00000436803.1:p.Asn683Thr
ENST00000528960.5:c.2237A>C	ENSP00000432914.1:p.Asn746Thr
ENST00000530764.1:n.44A>C
ENST00000533207.5:n.1721A>C
ENST00000534013.5:c.572A>C	ENSP00000436561.1:p.Asn191Thr
ENST00000534780.5:c.2354A>C	ENSP00000432352.1:p.Asn785Thr
ENST00000617858.4:c.2048A>C	ENSP00000481227.1:p.Asn683Thr
ENST00000619228.2:c.2237A>C	ENSP00000482698.1:p.Asn746Thr
NM_000926.4:c.2354A>C MANE Select	NP_000917.3:p.Asn785Thr
NM_001202474.3:c.1862A>C	NP_001189403.1:p.Asn621Thr
NM_001271161.2:c.1556A>C	NP_001258090.1:p.Asn519Thr
NM_001271162.1:c.572A>C	NP_001258091.1:p.Asn191Thr
NR_073141.2:n.2347A>C
NR_073142.2:n.2230A>C
NR_073143.2:n.2041A>C
XM_006718858.2:c.2354A>C	XP_006718921.1:p.Asn785Thr
XM_006718858.3:c.2354A>C	XP_006718921.1:p.Asn785Thr
NM_001271162.2:c.572A>C	NP_001258091.1:p.Asn191Thr
NR_073141.3:n.2361A>C
NR_073142.3:n.2244A>C
NR_073143.3:n.2055A>C