Canonical Allele Identifier: CA601634692

Gene: PGR

Linked Data

• dbSNP Id: rs1457182308
• gnomAD v2: 11-100967535-T-TC
• gnomAD v3: 11-101096804-T-TC
• gnomAD v4: 11-101096804-T-TC
• MyVariant Identifiers: chr11:g.100967535_100967536insC (hg19) ; chr11:g.101096804_101096805insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101096804_101096805insC , CM000673.2:g.101096804_101096805insC	GRCh38
NC_000011.9:g.100967535_100967536insC , CM000673.1:g.100967535_100967536insC	GRCh37
NC_000011.8:g.100472745_100472746insC	NCBI36
NG_016475.1:g.38009_38010insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.1790-4929_1790-4928insG MANE Select	ENSP00000325120.5:n.1790-4929_1790-4928insG
ENST00000263463.9:c.1790-4929_1790-4928insG	ENSP00000263463.5:n.1790-4929_1790-4928insG
ENST00000325455.9:c.1790-4929_1790-4928insG	ENSP00000325120.5:n.1790-4929_1790-4928insG
ENST00000526300.5:c.1790-4929_1790-4928insG	ENSP00000436803.1:n.1790-4929_1790-4928insG
ENST00000528960.5:c.1789+29202_1789+29203insG	ENSP00000432914.1:n.1789+29202_1789+29203insG
ENST00000534013.5:c.8-4929_8-4928insG	ENSP00000436561.1:n.8-4929_8-4928insG
ENST00000534780.5:c.1790-4929_1790-4928insG	ENSP00000432352.1:n.1790-4929_1790-4928insG
ENST00000617858.4:c.1790-4929_1790-4928insG	ENSP00000481227.1:n.1790-4929_1790-4928insG
ENST00000619228.2:c.1789+29202_1789+29203insG	ENSP00000482698.1:n.1789+29202_1789+29203insG
ENST00000632634.1:c.212-4929_212-4928insG	ENSP00000487607.1:n.212-4929_212-4928insG
NM_000926.4:c.1790-4929_1790-4928insG MANE Select	NP_000917.3:n.1790-4929_1790-4928insG
NM_001202474.3:c.1298-4929_1298-4928insG	NP_001189403.1:n.1298-4929_1298-4928insG
NM_001271161.2:c.1298-4929_1298-4928insG	NP_001258090.1:n.1298-4929_1298-4928insG
NM_001271162.1:c.8-4929_8-4928insG	NP_001258091.1:n.8-4929_8-4928insG
NR_073141.2:n.1783-4929_1783-4928insG
NR_073142.2:n.1782+29202_1782+29203insG
NR_073143.2:n.1783-4929_1783-4928insG
XM_006718858.2:c.1790-4929_1790-4928insG	XP_006718921.1:n.1790-4929_1790-4928insG
XR_947831.1:n.3362-4929_3362-4928insG
XM_006718858.3:c.1790-4929_1790-4928insG	XP_006718921.1:n.1790-4929_1790-4928insG
NM_001271162.2:c.8-4929_8-4928insG	NP_001258091.1:n.8-4929_8-4928insG
NR_073141.3:n.1797-4929_1797-4928insG
NR_073142.3:n.1796+29202_1796+29203insG
NR_073143.3:n.1797-4929_1797-4928insG