Canonical Allele Identifier: CA2615658393
Gene: PGR HGNC NCBI

Linked Data

gnomAD v4: 11-101034485-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101034485G>T , CM000673.2:g.101034485G>T GRCh38
NC_000011.9:g.100905216G>T , CM000673.1:g.100905216G>T GRCh37
NC_000011.8:g.100410426G>T NCBI36
NG_016475.1:g.100329C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.*4631C>A MANE Select ENSP00000325120.5:n.*4631C>A
ENST00000325455.9:c.*4631C>A ENSP00000325120.5:n.*4631C>A
NM_000926.4:c.*4631C>A MANE Select NP_000917.3:n.*4631C>A
NM_001202474.3:c.*4631C>A NP_001189403.1:n.*4631C>A
NM_001271161.2:c.*4631C>A NP_001258090.1:n.*4631C>A
NM_001271162.1:c.*4631C>A NP_001258091.1:n.*4631C>A
NR_073141.2:n.7374C>A
NR_073142.2:n.7257C>A
NR_073143.2:n.6989C>A
NM_001271162.2:c.*4631C>A NP_001258091.1:n.*4631C>A
NR_073141.3:n.7388C>A
NR_073142.3:n.7271C>A
NR_073143.3:n.7003C>A
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