Canonical Allele Identifier: CA941511014

Gene: PGR PGR-AS1

Linked Data

• dbSNP Id: rs1863031750
• gnomAD v3: 11-101129505-T-C
• gnomAD v4: 11-101129505-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101129505T>C , CM000673.2:g.101129505T>C	GRCh38
NC_000011.9:g.101000236T>C , CM000673.1:g.101000236T>C	GRCh37
NC_000011.8:g.100505446T>C	NCBI36
NG_016475.1:g.5309A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.-435A>G (PGR) MANE Select	ENSP00000325120.5:n.-435A>G
ENST00000325455.9:c.-435A>G (PGR)	ENSP00000325120.5:n.-435A>G
ENST00000534013.5:c.-223A>G (PGR)	ENSP00000436561.1:n.-223A>G
ENST00000617858.4:c.-435A>G (PGR)	ENSP00000481227.1:n.-435A>G
ENST00000619228.2:c.-435A>G (PGR)	ENSP00000482698.1:n.-435A>G
NM_000926.4:c.-435A>G (PGR) MANE Select	NP_000917.3:n.-435A>G
NM_001271162.1:c.-223A>G (PGR)	NP_001258091.1:n.-223A>G
NR_073144.1:n.429T>C (PGR-AS1)
XM_006718858.2:c.-435A>G (PGR)	XP_006718921.1:n.-435A>G
XM_011542869.1:c.-435A>G (PGR)	XP_011541171.1:n.-435A>G
XR_947831.1:n.1138A>G (PGR)
XM_006718858.3:c.-435A>G (PGR)	XP_006718921.1:n.-435A>G
XM_011542869.2:c.-435A>G (PGR)	XP_011541171.1:n.-435A>G
NM_001271162.2:c.-223A>G (PGR)	NP_001258091.1:n.-223A>G