Canonical Allele Identifier: CA2615658489

Gene: PGR

Linked Data

• gnomAD v4: 11-101034740-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034740C>A , CM000673.2:g.101034740C>A	GRCh38
NC_000011.9:g.100905471C>A , CM000673.1:g.100905471C>A	GRCh37
NC_000011.8:g.100410681C>A	NCBI36
NG_016475.1:g.100074G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4376G>T MANE Select	ENSP00000325120.5:n.*4376G>T
ENST00000325455.9:c.*4376G>T	ENSP00000325120.5:n.*4376G>T
NM_000926.4:c.*4376G>T MANE Select	NP_000917.3:n.*4376G>T
NM_001202474.3:c.*4376G>T	NP_001189403.1:n.*4376G>T
NM_001271161.2:c.*4376G>T	NP_001258090.1:n.*4376G>T
NM_001271162.1:c.*4376G>T	NP_001258091.1:n.*4376G>T
NR_073141.2:n.7119G>T
NR_073142.2:n.7002G>T
NR_073143.2:n.6734G>T
NM_001271162.2:c.*4376G>T	NP_001258091.1:n.*4376G>T
NR_073141.3:n.7133G>T
NR_073142.3:n.7016G>T
NR_073143.3:n.6748G>T