Canonical Allele Identifier: CA382436363

Gene: PGR

Linked Data

• gnomAD v4: 11-101051559-T-G
• MyVariant Identifiers: chr11:g.100922290T>G (hg19) ; chr11:g.101051559T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051559T>G , CM000673.2:g.101051559T>G	GRCh38
NC_000011.9:g.100922290T>G , CM000673.1:g.100922290T>G	GRCh37
NC_000011.8:g.100427500T>G	NCBI36
NG_016475.1:g.83255A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2222A>C MANE Select	ENSP00000325120.5:p.Asn741Thr
ENST00000263463.9:c.1916A>C	ENSP00000263463.5:p.Asn639Thr
ENST00000325455.9:c.2222A>C	ENSP00000325120.5:p.Asn741Thr
ENST00000526300.5:c.1916A>C	ENSP00000436803.1:p.Asn639Thr
ENST00000528960.5:c.2105A>C	ENSP00000432914.1:p.Asn702Thr
ENST00000533207.5:n.1589A>C
ENST00000534013.5:c.440A>C	ENSP00000436561.1:p.Asn147Thr
ENST00000534780.5:c.2222A>C	ENSP00000432352.1:p.Asn741Thr
ENST00000617858.4:c.1916A>C	ENSP00000481227.1:p.Asn639Thr
ENST00000619228.2:c.2105A>C	ENSP00000482698.1:p.Asn702Thr
NM_000926.4:c.2222A>C MANE Select	NP_000917.3:p.Asn741Thr
NM_001202474.3:c.1730A>C	NP_001189403.1:p.Asn577Thr
NM_001271161.2:c.1424A>C	NP_001258090.1:p.Asn475Thr
NM_001271162.1:c.440A>C	NP_001258091.1:p.Asn147Thr
NR_073141.2:n.2215A>C
NR_073142.2:n.2098A>C
NR_073143.2:n.1909A>C
XM_006718858.2:c.2222A>C	XP_006718921.1:p.Asn741Thr
XR_947831.1:n.3903A>C
XM_006718858.3:c.2222A>C	XP_006718921.1:p.Asn741Thr
NM_001271162.2:c.440A>C	NP_001258091.1:p.Asn147Thr
NR_073141.3:n.2229A>C
NR_073142.3:n.2112A>C
NR_073143.3:n.1923A>C