Canonical Allele Identifier: CA2615679972

Gene: PGR

Linked Data

• gnomAD v4: 11-101051681-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051681T>A , CM000673.2:g.101051681T>A	GRCh38
NC_000011.9:g.100922412T>A , CM000673.1:g.100922412T>A	GRCh37
NC_000011.8:g.100427622T>A	NCBI36
NG_016475.1:g.83133A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2213-113A>T MANE Select	ENSP00000325120.5:n.2213-113A>T
ENST00000263463.9:c.1907-113A>T	ENSP00000263463.5:n.1907-113A>T
ENST00000325455.9:c.2213-113A>T	ENSP00000325120.5:n.2213-113A>T
ENST00000526300.5:c.1907-113A>T	ENSP00000436803.1:n.1907-113A>T
ENST00000528960.5:c.2096-113A>T	ENSP00000432914.1:n.2096-113A>T
ENST00000533207.5:n.1580-113A>T
ENST00000534013.5:c.431-113A>T	ENSP00000436561.1:n.431-113A>T
ENST00000534780.5:c.2213-113A>T	ENSP00000432352.1:n.2213-113A>T
ENST00000617858.4:c.1907-113A>T	ENSP00000481227.1:n.1907-113A>T
ENST00000619228.2:c.2096-113A>T	ENSP00000482698.1:n.2096-113A>T
NM_000926.4:c.2213-113A>T MANE Select	NP_000917.3:n.2213-113A>T
NM_001202474.3:c.1721-113A>T	NP_001189403.1:n.1721-113A>T
NM_001271161.2:c.1415-113A>T	NP_001258090.1:n.1415-113A>T
NM_001271162.1:c.431-113A>T	NP_001258091.1:n.431-113A>T
NR_073141.2:n.2206-113A>T
NR_073142.2:n.2089-113A>T
NR_073143.2:n.1900-113A>T
XM_006718858.2:c.2213-113A>T	XP_006718921.1:n.2213-113A>T
XR_947831.1:n.3894-113A>T
XM_006718858.3:c.2213-113A>T	XP_006718921.1:n.2213-113A>T
NM_001271162.2:c.431-113A>T	NP_001258091.1:n.431-113A>T
NR_073141.3:n.2220-113A>T
NR_073142.3:n.2103-113A>T
NR_073143.3:n.1914-113A>T