Canonical Allele Identifier: CA2615682189

Gene: PGR PGR-AS1

Linked Data

• gnomAD v4: 11-101129491-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101129491C>T , CM000673.2:g.101129491C>T	GRCh38
NC_000011.9:g.101000222C>T , CM000673.1:g.101000222C>T	GRCh37
NC_000011.8:g.100505432C>T	NCBI36
NG_016475.1:g.5323G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.-421G>A (PGR) MANE Select	ENSP00000325120.5:n.-421G>A
ENST00000325455.9:c.-421G>A (PGR)	ENSP00000325120.5:n.-421G>A
ENST00000534013.5:c.-209G>A (PGR)	ENSP00000436561.1:n.-209G>A
ENST00000617858.4:c.-421G>A (PGR)	ENSP00000481227.1:n.-421G>A
ENST00000619228.2:c.-421G>A (PGR)	ENSP00000482698.1:n.-421G>A
NM_000926.4:c.-421G>A (PGR) MANE Select	NP_000917.3:n.-421G>A
NM_001271162.1:c.-209G>A (PGR)	NP_001258091.1:n.-209G>A
NR_073144.1:n.415C>T (PGR-AS1)
XM_006718858.2:c.-421G>A (PGR)	XP_006718921.1:n.-421G>A
XM_011542869.1:c.-421G>A (PGR)	XP_011541171.1:n.-421G>A
XR_947831.1:n.1152G>A (PGR)
XM_006718858.3:c.-421G>A (PGR)	XP_006718921.1:n.-421G>A
XM_011542869.2:c.-421G>A (PGR)	XP_011541171.1:n.-421G>A
NM_001271162.2:c.-209G>A (PGR)	NP_001258091.1:n.-209G>A