Canonical Allele Identifier: CA228192219
Gene: PGR HGNC NCBI

Linked Data

dbSNP Id: rs72547494

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101096849_101096851del , CM000673.2:g.101096849_101096851del GRCh38
NC_000011.9:g.100967580_100967582del , CM000673.1:g.100967580_100967582del GRCh37
NC_000011.8:g.100472790_100472792del NCBI36
NG_016475.1:g.37967_37969del

Transcript Alleles

HGVS Amino-acid change
ENST00000325455.10:c.1790-4971_1790-4969del MANE Select ENSP00000325120.5:n.1790-4971_1790-4969de...
ENST00000263463.9:c.1790-4971_1790-4969del ENSP00000263463.5:n.1790-4971_1790-4969de...
ENST00000325455.9:c.1790-4971_1790-4969del ENSP00000325120.5:n.1790-4971_1790-4969de...
ENST00000526300.5:c.1790-4971_1790-4969del ENSP00000436803.1:n.1790-4971_1790-4969de...
ENST00000528960.5:c.1789+29160_1789+29162del ENSP00000432914.1:n.1789+29160_1789+29162...
ENST00000534013.5:c.8-4971_8-4969del ENSP00000436561.1:n.8-4971_8-4969del
ENST00000534780.5:c.1790-4971_1790-4969del ENSP00000432352.1:n.1790-4971_1790-4969de...
ENST00000617858.4:c.1790-4971_1790-4969del ENSP00000481227.1:n.1790-4971_1790-4969de...
ENST00000619228.2:c.1789+29160_1789+29162del ENSP00000482698.1:n.1789+29160_1789+29162...
ENST00000632634.1:c.212-4971_212-4969del ENSP00000487607.1:n.212-4971_212-4969del
NM_000926.4:c.1790-4971_1790-4969del MANE Select NP_000917.3:n.1790-4971_1790-4969del
NM_001202474.3:c.1298-4971_1298-4969del NP_001189403.1:n.1298-4971_1298-4969del
NM_001271161.2:c.1298-4971_1298-4969del NP_001258090.1:n.1298-4971_1298-4969del
NM_001271162.1:c.8-4971_8-4969del NP_001258091.1:n.8-4971_8-4969del
NR_073141.2:n.1783-4971_1783-4969del
NR_073142.2:n.1782+29160_1782+29162del
NR_073143.2:n.1783-4971_1783-4969del
XM_006718858.2:c.1790-4971_1790-4969del XP_006718921.1:n.1790-4971_1790-4969del
XR_947831.1:n.3362-4971_3362-4969del
XM_006718858.3:c.1790-4971_1790-4969del XP_006718921.1:n.1790-4971_1790-4969del
NM_001271162.2:c.8-4971_8-4969del NP_001258091.1:n.8-4971_8-4969del
NR_073141.3:n.1797-4971_1797-4969del
NR_073142.3:n.1796+29160_1796+29162del
NR_073143.3:n.1797-4971_1797-4969del