Canonical Allele Identifier: CA382436338

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922280A>C (hg19) ; chr11:g.101051549A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051549A>C , CM000673.2:g.101051549A>C	GRCh38
NC_000011.9:g.100922280A>C , CM000673.1:g.100922280A>C	GRCh37
NC_000011.8:g.100427490A>C	NCBI36
NG_016475.1:g.83265T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2232T>G MANE Select	ENSP00000325120.5:p.Ile744Met
ENST00000263463.9:c.1926T>G	ENSP00000263463.5:p.Ile642Met
ENST00000325455.9:c.2232T>G	ENSP00000325120.5:p.Ile744Met
ENST00000526300.5:c.1926T>G	ENSP00000436803.1:p.Ile642Met
ENST00000528960.5:c.2115T>G	ENSP00000432914.1:p.Ile705Met
ENST00000533207.5:n.1599T>G
ENST00000534013.5:c.450T>G	ENSP00000436561.1:p.Ile150Met
ENST00000534780.5:c.2232T>G	ENSP00000432352.1:p.Ile744Met
ENST00000617858.4:c.1926T>G	ENSP00000481227.1:p.Ile642Met
ENST00000619228.2:c.2115T>G	ENSP00000482698.1:p.Ile705Met
NM_000926.4:c.2232T>G MANE Select	NP_000917.3:p.Ile744Met
NM_001202474.3:c.1740T>G	NP_001189403.1:p.Ile580Met
NM_001271161.2:c.1434T>G	NP_001258090.1:p.Ile478Met
NM_001271162.1:c.450T>G	NP_001258091.1:p.Ile150Met
NR_073141.2:n.2225T>G
NR_073142.2:n.2108T>G
NR_073143.2:n.1919T>G
XM_006718858.2:c.2232T>G	XP_006718921.1:p.Ile744Met
XR_947831.1:n.3913T>G
XM_006718858.3:c.2232T>G	XP_006718921.1:p.Ile744Met
NM_001271162.2:c.450T>G	NP_001258091.1:p.Ile150Met
NR_073141.3:n.2239T>G
NR_073142.3:n.2122T>G
NR_073143.3:n.1933T>G