Canonical Allele Identifier: CA382436865

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100933327A>T (hg19) ; chr11:g.101062596A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062596A>T , CM000673.2:g.101062596A>T	GRCh38
NC_000011.9:g.100933327A>T , CM000673.1:g.100933327A>T	GRCh37
NC_000011.8:g.100438537A>T	NCBI36
NG_016475.1:g.72218T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2063T>A MANE Select	ENSP00000325120.5:p.Ile688Asn
ENST00000263463.9:c.1907-11028T>A	ENSP00000263463.5:n.1907-11028T>A
ENST00000325455.9:c.2063T>A	ENSP00000325120.5:p.Ile688Asn
ENST00000526300.5:c.1907-11028T>A	ENSP00000436803.1:n.1907-11028T>A
ENST00000528960.5:c.1946T>A	ENSP00000432914.1:p.Ile649Asn
ENST00000533207.5:n.1430T>A
ENST00000534013.5:c.281T>A	ENSP00000436561.1:p.Ile94Asn
ENST00000534780.5:c.2063T>A	ENSP00000432352.1:p.Ile688Asn
ENST00000617858.4:c.1907-11028T>A	ENSP00000481227.1:n.1907-11028T>A
ENST00000619228.2:c.1946T>A	ENSP00000482698.1:p.Ile649Asn
ENST00000632634.1:c.485T>A	ENSP00000487607.1:p.Ile162Asn
NM_000926.4:c.2063T>A MANE Select	NP_000917.3:p.Ile688Asn
NM_001202474.3:c.1571T>A	NP_001189403.1:p.Ile524Asn
NM_001271161.2:c.1415-11028T>A	NP_001258090.1:n.1415-11028T>A
NM_001271162.1:c.281T>A	NP_001258091.1:p.Ile94Asn
NR_073141.2:n.2056T>A
NR_073142.2:n.1939T>A
NR_073143.2:n.1900-11028T>A
XM_006718858.2:c.2063T>A	XP_006718921.1:p.Ile688Asn
XR_947831.1:n.3635T>A
XM_006718858.3:c.2063T>A	XP_006718921.1:p.Ile688Asn
NM_001271162.2:c.281T>A	NP_001258091.1:p.Ile94Asn
NR_073141.3:n.2070T>A
NR_073142.3:n.1953T>A
NR_073143.3:n.1914-11028T>A