Canonical Allele Identifier: CA1995637279

Gene: PGR

Linked Data

• dbSNP Id: rs1859458169

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101034840_101034846del , CM000673.2:g.101034840_101034846del	GRCh38
NC_000011.9:g.100905571_100905577del , CM000673.1:g.100905571_100905577del	GRCh37
NC_000011.8:g.100410781_100410787del	NCBI36
NG_016475.1:g.99971_99977del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.*4273_*4279del MANE Select	ENSP00000325120.5:n.*4273_*4279del
ENST00000325455.9:c.*4273_*4279del	ENSP00000325120.5:n.*4273_*4279del
NM_000926.4:c.*4273_*4279del MANE Select	NP_000917.3:n.*4273_*4279del
NM_001202474.3:c.*4273_*4279del	NP_001189403.1:n.*4273_*4279del
NM_001271161.2:c.*4273_*4279del	NP_001258090.1:n.*4273_*4279del
NM_001271162.1:c.*4273_*4279del	NP_001258091.1:n.*4273_*4279del
NR_073141.2:n.7016_7022del
NR_073142.2:n.6899_6905del
NR_073143.2:n.6631_6637del
NM_001271162.2:c.*4273_*4279del	NP_001258091.1:n.*4273_*4279del
NR_073141.3:n.7030_7036del
NR_073142.3:n.6913_6919del
NR_073143.3:n.6645_6651del