Canonical Allele Identifier: CA2615682200

Gene: PGR PGR-AS1

Linked Data

• gnomAD v4: 11-101129500-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101129500T>G , CM000673.2:g.101129500T>G	GRCh38
NC_000011.9:g.101000231T>G , CM000673.1:g.101000231T>G	GRCh37
NC_000011.8:g.100505441T>G	NCBI36
NG_016475.1:g.5314A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.-430A>C (PGR) MANE Select	ENSP00000325120.5:n.-430A>C
ENST00000325455.9:c.-430A>C (PGR)	ENSP00000325120.5:n.-430A>C
ENST00000534013.5:c.-218A>C (PGR)	ENSP00000436561.1:n.-218A>C
ENST00000617858.4:c.-430A>C (PGR)	ENSP00000481227.1:n.-430A>C
ENST00000619228.2:c.-430A>C (PGR)	ENSP00000482698.1:n.-430A>C
NM_000926.4:c.-430A>C (PGR) MANE Select	NP_000917.3:n.-430A>C
NM_001271162.1:c.-218A>C (PGR)	NP_001258091.1:n.-218A>C
NR_073144.1:n.424T>G (PGR-AS1)
XM_006718858.2:c.-430A>C (PGR)	XP_006718921.1:n.-430A>C
XM_011542869.1:c.-430A>C (PGR)	XP_011541171.1:n.-430A>C
XR_947831.1:n.1143A>C (PGR)
XM_006718858.3:c.-430A>C (PGR)	XP_006718921.1:n.-430A>C
XM_011542869.2:c.-430A>C (PGR)	XP_011541171.1:n.-430A>C
NM_001271162.2:c.-218A>C (PGR)	NP_001258091.1:n.-218A>C