Canonical Allele Identifier: CA2615679909

Gene: PGR

Linked Data

• gnomAD v4: 11-101051499-A-AAC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051502_101051503dup , CM000673.2:g.101051502_101051503dup	GRCh38
NC_000011.9:g.100922233_100922234dup , CM000673.1:g.100922233_100922234dup	GRCh37
NC_000011.8:g.100427443_100427444dup	NCBI36
NG_016475.1:g.83313_83314dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2280_2281dup MANE Select	ENSP00000325120.5:p.Phe761CysfsTer4
ENST00000263463.9:c.1974_1975dup	ENSP00000263463.5:p.Phe659CysfsTer4
ENST00000325455.9:c.2280_2281dup	ENSP00000325120.5:p.Phe761CysfsTer4
ENST00000526300.5:c.1974_1975dup	ENSP00000436803.1:p.Phe659CysfsTer4
ENST00000528960.5:c.2163_2164dup	ENSP00000432914.1:p.Phe722CysfsTer4
ENST00000533207.5:n.1647_1648dup
ENST00000534013.5:c.498_499dup	ENSP00000436561.1:p.Phe167CysfsTer4
ENST00000534780.5:c.2280_2281dup	ENSP00000432352.1:p.Phe761CysfsTer4
ENST00000617858.4:c.1974_1975dup	ENSP00000481227.1:p.Phe659CysfsTer4
ENST00000619228.2:c.2163_2164dup	ENSP00000482698.1:p.Phe722CysfsTer4
NM_000926.4:c.2280_2281dup MANE Select	NP_000917.3:p.Phe761CysfsTer4
NM_001202474.3:c.1788_1789dup	NP_001189403.1:p.Phe597CysfsTer4
NM_001271161.2:c.1482_1483dup	NP_001258090.1:p.Phe495CysfsTer4
NM_001271162.1:c.498_499dup	NP_001258091.1:p.Phe167CysfsTer4
NR_073141.2:n.2273_2274dup
NR_073142.2:n.2156_2157dup
NR_073143.2:n.1967_1968dup
XM_006718858.2:c.2280_2281dup	XP_006718921.1:p.Phe761CysfsTer4
XR_947831.1:n.3961_3962dup
XM_006718858.3:c.2280_2281dup	XP_006718921.1:p.Phe761CysfsTer4
NM_001271162.2:c.498_499dup	NP_001258091.1:p.Phe167CysfsTer4
NR_073141.3:n.2287_2288dup
NR_073142.3:n.2170_2171dup
NR_073143.3:n.1981_1982dup