Canonical Allele Identifier: CA227527249

Gene: PGR

Linked Data

• dbSNP Id: rs35131968
• MyVariant Identifiers: chr11:g.100922157_100922158insT (hg19) ; chr11:g.101051426_101051427insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101051429dup , CM000673.2:g.101051429dup	GRCh38
NC_000011.9:g.100922160dup , CM000673.1:g.100922160dup	GRCh37
NC_000011.8:g.100427370dup	NCBI36
NG_016475.1:g.83387dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000325455.10:c.2354dup MANE Select	ENSP00000325120.5:p.Asn785LysfsTer2
ENST00000263463.9:c.2048dup	ENSP00000263463.5:p.Asn683LysfsTer2
ENST00000325455.9:c.2354dup	ENSP00000325120.5:p.Asn785LysfsTer2
ENST00000526300.5:c.2048dup	ENSP00000436803.1:p.Asn683LysfsTer2
ENST00000528960.5:c.2237dup	ENSP00000432914.1:p.Asn746LysfsTer2
ENST00000530764.1:n.44dup
ENST00000533207.5:n.1721dup
ENST00000534013.5:c.572dup	ENSP00000436561.1:p.Asn191LysfsTer2
ENST00000534780.5:c.2354dup	ENSP00000432352.1:p.Asn785LysfsTer2
ENST00000617858.4:c.2048dup	ENSP00000481227.1:p.Asn683LysfsTer2
ENST00000619228.2:c.2237dup	ENSP00000482698.1:p.Asn746LysfsTer2
NM_000926.4:c.2354dup MANE Select	NP_000917.3:p.Asn785LysfsTer2
NM_001202474.3:c.1862dup	NP_001189403.1:p.Asn621LysfsTer2
NM_001271161.2:c.1556dup	NP_001258090.1:p.Asn519LysfsTer2
NM_001271162.1:c.572dup	NP_001258091.1:p.Asn191LysfsTer2
NR_073141.2:n.2347dup
NR_073142.2:n.2230dup
NR_073143.2:n.2041dup
XM_006718858.2:c.2354dup	XP_006718921.1:p.Asn785LysfsTer2
XM_006718858.3:c.2354dup	XP_006718921.1:p.Asn785LysfsTer2
NM_001271162.2:c.572dup	NP_001258091.1:p.Asn191LysfsTer2
NR_073141.3:n.2361dup
NR_073142.3:n.2244dup
NR_073143.3:n.2055dup