Canonical Allele Identifier: CA2615658515

Gene: PGR

Linked Data

• gnomAD v4: 11-101034825-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034825T>C , CM000673.2:g.101034825T>C	GRCh38
NC_000011.9:g.100905556T>C , CM000673.1:g.100905556T>C	GRCh37
NC_000011.8:g.100410766T>C	NCBI36
NG_016475.1:g.99989A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4291A>G MANE Select	ENSP00000325120.5:n.*4291A>G
ENST00000325455.9:c.*4291A>G	ENSP00000325120.5:n.*4291A>G
NM_000926.4:c.*4291A>G MANE Select	NP_000917.3:n.*4291A>G
NM_001202474.3:c.*4291A>G	NP_001189403.1:n.*4291A>G
NM_001271161.2:c.*4291A>G	NP_001258090.1:n.*4291A>G
NM_001271162.1:c.*4291A>G	NP_001258091.1:n.*4291A>G
NR_073141.2:n.7034A>G
NR_073142.2:n.6917A>G
NR_073143.2:n.6649A>G
NM_001271162.2:c.*4291A>G	NP_001258091.1:n.*4291A>G
NR_073141.3:n.7048A>G
NR_073142.3:n.6931A>G
NR_073143.3:n.6663A>G