Canonical Allele Identifier: CA2615682080

Gene: PGR PGR-AS1

Linked Data

• gnomAD v4: 11-101129390-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101129390C>A , CM000673.2:g.101129390C>A	GRCh38
NC_000011.9:g.101000121C>A , CM000673.1:g.101000121C>A	GRCh37
NC_000011.8:g.100505331C>A	NCBI36
NG_016475.1:g.5424G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.-320G>T (PGR) MANE Select	ENSP00000325120.5:n.-320G>T
ENST00000325455.9:c.-320G>T (PGR)	ENSP00000325120.5:n.-320G>T
ENST00000534013.5:c.-146+38G>T (PGR)	ENSP00000436561.1:n.-146+38G>T
ENST00000617858.4:c.-320G>T (PGR)	ENSP00000481227.1:n.-320G>T
ENST00000619228.2:c.-320G>T (PGR)	ENSP00000482698.1:n.-320G>T
NM_000926.4:c.-320G>T (PGR) MANE Select	NP_000917.3:n.-320G>T
NM_001271162.1:c.-146+38G>T (PGR)	NP_001258091.1:n.-146+38G>T
NR_073144.1:n.314C>A (PGR-AS1)
XM_006718858.2:c.-320G>T (PGR)	XP_006718921.1:n.-320G>T
XM_011542869.1:c.-320G>T (PGR)	XP_011541171.1:n.-320G>T
XR_947831.1:n.1253G>T (PGR)
XM_006718858.3:c.-320G>T (PGR)	XP_006718921.1:n.-320G>T
XM_011542869.2:c.-320G>T (PGR)	XP_011541171.1:n.-320G>T
NM_001271162.2:c.-146+38G>T (PGR)	NP_001258091.1:n.-146+38G>T