Canonical Allele Identifier: CA382437157

Gene: PGR

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101062681C>T , CM000673.2:g.101062681C>T	GRCh38
NC_000011.9:g.100933412C>T , CM000673.1:g.100933412C>T	GRCh37
NC_000011.8:g.100438622C>T	NCBI36
NG_016475.1:g.72133G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000926.4:c.1978G>A MANE Select	NP_000917.3:p.Val660Met
ENST00000325455.10:c.1978G>A MANE Select	ENSP00000325120.5:p.Val660Met
NM_001202474.3:c.1486G>A	NP_001189403.1:p.Val496Met
NM_001271161.2:c.1415-11113G>A	NP_001258090.1:n.1415-11113G>A
NM_001271162.1:c.196G>A	NP_001258091.1:p.Val66Met
NM_001271162.2:c.196G>A	NP_001258091.1:p.Val66Met
NR_073141.2:n.1971G>A
NR_073141.3:n.1985G>A
NR_073142.2:n.1854G>A
NR_073142.3:n.1868G>A
NR_073143.2:n.1900-11113G>A
NR_073143.3:n.1914-11113G>A
ENST00000263463.9:c.1907-11113G>A	ENSP00000263463.5:n.1907-11113G>A
ENST00000325455.9:c.1978G>A	ENSP00000325120.5:p.Val660Met
ENST00000526300.5:c.1907-11113G>A	ENSP00000436803.1:n.1907-11113G>A
ENST00000528960.5:c.1861G>A	ENSP00000432914.1:p.Val621Met
ENST00000533207.5:n.1345G>A
ENST00000534013.5:c.196G>A	ENSP00000436561.1:p.Val66Met
ENST00000534780.5:c.1978G>A	ENSP00000432352.1:p.Val660Met
ENST00000617858.4:c.1907-11113G>A	ENSP00000481227.1:n.1907-11113G>A
ENST00000619228.2:c.1861G>A	ENSP00000482698.1:p.Val621Met
ENST00000632634.1:c.400G>A	ENSP00000487607.1:p.Val134Met
XM_006718858.2:c.1978G>A	XP_006718921.1:p.Val660Met
XM_006718858.3:c.1978G>A	XP_006718921.1:p.Val660Met
XR_947831.1:n.3550G>A