Canonical Allele Identifier: CA382436229

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922236A>C (hg19) ; chr11:g.101051505A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051505A>C , CM000673.2:g.101051505A>C	GRCh38
NC_000011.9:g.100922236A>C , CM000673.1:g.100922236A>C	GRCh37
NC_000011.8:g.100427446A>C	NCBI36
NG_016475.1:g.83309T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2276T>G MANE Select	ENSP00000325120.5:p.Met759Arg
ENST00000263463.9:c.1970T>G	ENSP00000263463.5:p.Met657Arg
ENST00000325455.9:c.2276T>G	ENSP00000325120.5:p.Met759Arg
ENST00000526300.5:c.1970T>G	ENSP00000436803.1:p.Met657Arg
ENST00000528960.5:c.2159T>G	ENSP00000432914.1:p.Met720Arg
ENST00000533207.5:n.1643T>G
ENST00000534013.5:c.494T>G	ENSP00000436561.1:p.Met165Arg
ENST00000534780.5:c.2276T>G	ENSP00000432352.1:p.Met759Arg
ENST00000617858.4:c.1970T>G	ENSP00000481227.1:p.Met657Arg
ENST00000619228.2:c.2159T>G	ENSP00000482698.1:p.Met720Arg
NM_000926.4:c.2276T>G MANE Select	NP_000917.3:p.Met759Arg
NM_001202474.3:c.1784T>G	NP_001189403.1:p.Met595Arg
NM_001271161.2:c.1478T>G	NP_001258090.1:p.Met493Arg
NM_001271162.1:c.494T>G	NP_001258091.1:p.Met165Arg
NR_073141.2:n.2269T>G
NR_073142.2:n.2152T>G
NR_073143.2:n.1963T>G
XM_006718858.2:c.2276T>G	XP_006718921.1:p.Met759Arg
XR_947831.1:n.3957T>G
XM_006718858.3:c.2276T>G	XP_006718921.1:p.Met759Arg
NM_001271162.2:c.494T>G	NP_001258091.1:p.Met165Arg
NR_073141.3:n.2283T>G
NR_073142.3:n.2166T>G
NR_073143.3:n.1977T>G