Canonical Allele Identifier: CA2615658462

Gene: PGR

Linked Data

• gnomAD v4: 11-101034626-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034626G>T , CM000673.2:g.101034626G>T	GRCh38
NC_000011.9:g.100905357G>T , CM000673.1:g.100905357G>T	GRCh37
NC_000011.8:g.100410567G>T	NCBI36
NG_016475.1:g.100188C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4490C>A MANE Select	ENSP00000325120.5:n.*4490C>A
ENST00000325455.9:c.*4490C>A	ENSP00000325120.5:n.*4490C>A
NM_000926.4:c.*4490C>A MANE Select	NP_000917.3:n.*4490C>A
NM_001202474.3:c.*4490C>A	NP_001189403.1:n.*4490C>A
NM_001271161.2:c.*4490C>A	NP_001258090.1:n.*4490C>A
NM_001271162.1:c.*4490C>A	NP_001258091.1:n.*4490C>A
NR_073141.2:n.7233C>A
NR_073142.2:n.7116C>A
NR_073143.2:n.6848C>A
NM_001271162.2:c.*4490C>A	NP_001258091.1:n.*4490C>A
NR_073141.3:n.7247C>A
NR_073142.3:n.7130C>A
NR_073143.3:n.6862C>A