Canonical Allele Identifier: CA382436310

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922269A>G (hg19) ; chr11:g.101051538A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051538A>G , CM000673.2:g.101051538A>G	GRCh38
NC_000011.9:g.100922269A>G , CM000673.1:g.100922269A>G	GRCh37
NC_000011.8:g.100427479A>G	NCBI36
NG_016475.1:g.83276T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2243T>C MANE Select	ENSP00000325120.5:p.Ile748Thr
ENST00000263463.9:c.1937T>C	ENSP00000263463.5:p.Ile646Thr
ENST00000325455.9:c.2243T>C	ENSP00000325120.5:p.Ile748Thr
ENST00000526300.5:c.1937T>C	ENSP00000436803.1:p.Ile646Thr
ENST00000528960.5:c.2126T>C	ENSP00000432914.1:p.Ile709Thr
ENST00000533207.5:n.1610T>C
ENST00000534013.5:c.461T>C	ENSP00000436561.1:p.Ile154Thr
ENST00000534780.5:c.2243T>C	ENSP00000432352.1:p.Ile748Thr
ENST00000617858.4:c.1937T>C	ENSP00000481227.1:p.Ile646Thr
ENST00000619228.2:c.2126T>C	ENSP00000482698.1:p.Ile709Thr
NM_000926.4:c.2243T>C MANE Select	NP_000917.3:p.Ile748Thr
NM_001202474.3:c.1751T>C	NP_001189403.1:p.Ile584Thr
NM_001271161.2:c.1445T>C	NP_001258090.1:p.Ile482Thr
NM_001271162.1:c.461T>C	NP_001258091.1:p.Ile154Thr
NR_073141.2:n.2236T>C
NR_073142.2:n.2119T>C
NR_073143.2:n.1930T>C
XM_006718858.2:c.2243T>C	XP_006718921.1:p.Ile748Thr
XR_947831.1:n.3924T>C
XM_006718858.3:c.2243T>C	XP_006718921.1:p.Ile748Thr
NM_001271162.2:c.461T>C	NP_001258091.1:p.Ile154Thr
NR_073141.3:n.2250T>C
NR_073142.3:n.2133T>C
NR_073143.3:n.1944T>C