Canonical Allele Identifier: CA476545581

Gene: PGR

Linked Data

• MyVariant Identifiers: chr11:g.100933332T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062601T>A , CM000673.2:g.101062601T>A	GRCh38
NC_000011.9:g.100933332T>A , CM000673.1:g.100933332T>A	GRCh37
NC_000011.8:g.100438542T>A	NCBI36
NG_016475.1:g.72213A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325455.10:c.2058A>T MANE Select	ENSP00000325120.5:p.Pro686=
ENST00000263463.9:c.1907-11033A>T	ENSP00000263463.5:n.1907-11033A>T
ENST00000325455.9:c.2058A>T	ENSP00000325120.5:p.Pro686=
ENST00000526300.5:c.1907-11033A>T	ENSP00000436803.1:n.1907-11033A>T
ENST00000528960.5:c.1941A>T	ENSP00000432914.1:p.Pro647=
ENST00000533207.5:n.1425A>T
ENST00000534013.5:c.276A>T	ENSP00000436561.1:p.Pro92=
ENST00000534780.5:c.2058A>T	ENSP00000432352.1:p.Pro686=
ENST00000617858.4:c.1907-11033A>T	ENSP00000481227.1:n.1907-11033A>T
ENST00000619228.2:c.1941A>T	ENSP00000482698.1:p.Pro647=
ENST00000632634.1:c.480A>T	ENSP00000487607.1:p.Pro160=
NM_000926.4:c.2058A>T MANE Select	NP_000917.3:p.Pro686=
NM_001202474.3:c.1566A>T	NP_001189403.1:p.Pro522=
NM_001271161.2:c.1415-11033A>T	NP_001258090.1:n.1415-11033A>T
NM_001271162.1:c.276A>T	NP_001258091.1:p.Pro92=
NR_073141.2:n.2051A>T
NR_073142.2:n.1934A>T
NR_073143.2:n.1900-11033A>T
XM_006718858.2:c.2058A>T	XP_006718921.1:p.Pro686=
XR_947831.1:n.3630A>T
XM_006718858.3:c.2058A>T	XP_006718921.1:p.Pro686=
NM_001271162.2:c.276A>T	NP_001258091.1:p.Pro92=
NR_073141.3:n.2065A>T
NR_073142.3:n.1948A>T
NR_073143.3:n.1914-11033A>T