Canonical Allele Identifier: CA382436057

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100922159T>C (hg19) ; chr11:g.101051428T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051428T>C , CM000673.2:g.101051428T>C	GRCh38
NC_000011.9:g.100922159T>C , CM000673.1:g.100922159T>C	GRCh37
NC_000011.8:g.100427369T>C	NCBI36
NG_016475.1:g.83386A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.2353A>G MANE Select	ENSP00000325120.5:p.Asn785Asp
ENST00000263463.9:c.2047A>G	ENSP00000263463.5:p.Asn683Asp
ENST00000325455.9:c.2353A>G	ENSP00000325120.5:p.Asn785Asp
ENST00000526300.5:c.2047A>G	ENSP00000436803.1:p.Asn683Asp
ENST00000528960.5:c.2236A>G	ENSP00000432914.1:p.Asn746Asp
ENST00000530764.1:n.43A>G
ENST00000533207.5:n.1720A>G
ENST00000534013.5:c.571A>G	ENSP00000436561.1:p.Asn191Asp
ENST00000534780.5:c.2353A>G	ENSP00000432352.1:p.Asn785Asp
ENST00000617858.4:c.2047A>G	ENSP00000481227.1:p.Asn683Asp
ENST00000619228.2:c.2236A>G	ENSP00000482698.1:p.Asn746Asp
NM_000926.4:c.2353A>G MANE Select	NP_000917.3:p.Asn785Asp
NM_001202474.3:c.1861A>G	NP_001189403.1:p.Asn621Asp
NM_001271161.2:c.1555A>G	NP_001258090.1:p.Asn519Asp
NM_001271162.1:c.571A>G	NP_001258091.1:p.Asn191Asp
NR_073141.2:n.2346A>G
NR_073142.2:n.2229A>G
NR_073143.2:n.2040A>G
XM_006718858.2:c.2353A>G	XP_006718921.1:p.Asn785Asp
XM_006718858.3:c.2353A>G	XP_006718921.1:p.Asn785Asp
NM_001271162.2:c.571A>G	NP_001258091.1:p.Asn191Asp
NR_073141.3:n.2360A>G
NR_073142.3:n.2243A>G
NR_073143.3:n.2054A>G