Canonical Allele Identifier: CA1248601009

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688142G= , CM000664.2:g.48688142G=	GRCh38
NC_000002.11:g.48915281G= , CM000664.1:g.48915281G=	GRCh37
NC_000002.10:g.48768785G=	NCBI36
NG_008193.1:g.72600C=
NG_033050.1:g.163218G=
NG_008193.2:g.72600C=
NG_033050.2:g.163218G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.1655C= (LHCGR) MANE Select	ENSP00000294954.6:p.Ala552=
ENST00000294954.11:c.1655C= (LHCGR)	ENSP00000294954.6:p.Ala552=
ENST00000401907.5:c.948-3C= (LHCGR)	ENSP00000385406.1:n.948-3C=
ENST00000402114.6:c.3441+16462G= (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16462G=
ENST00000403273.5:c.*399C= (LHCGR)	ENSP00000385847.1:n.*399C=
ENST00000405626.5:c.1574C= (LHCGR)	ENSP00000386033.1:p.Ala525=
ENST00000508440.1:c.276+16462G= (GTF2A1L)	ENSP00000421474.1:n.276+16462G=
ENST00000602369.3:c.*220+6082C=	ENSP00000473498.1:n.*220+6082C=
NM_000233.3:c.1655C= (LHCGR)	NP_000224.2:p.Ala552=
NM_001198593.1:c.3441+16462G= (STON1-GTF2A1L)	NP_001185522.1:n.3441+16462G=
XM_005264309.2:c.698C= (LHCGR)	XP_005264366.1:p.Ala233=
XM_006712015.2:c.725C= (LHCGR)	XP_006712078.1:p.Ala242=
XM_011532828.1:c.1580C= (LHCGR)	XP_011531130.1:p.Ala527=
XM_011532829.1:c.1394C= (LHCGR)	XP_011531131.1:p.Ala465=
XM_011532830.1:c.1313C= (LHCGR)	XP_011531132.1:p.Ala438=
XM_011532831.1:c.1019C= (LHCGR)	XP_011531133.1:p.Ala340=
XM_011532832.1:c.725C= (LHCGR)	XP_011531134.1:p.Ala242=
XM_011532833.1:c.725C= (LHCGR)	XP_011531135.1:p.Ala242=
XM_011532834.1:c.698C= (LHCGR)	XP_011531136.1:p.Ala233=
XM_005264309.3:c.698C= (LHCGR)	XP_005264366.1:p.Ala233=
XM_006712015.3:c.725C= (LHCGR)	XP_006712078.1:p.Ala242=
XM_011532834.2:c.698C= (LHCGR)	XP_011531136.1:p.Ala233=
XM_017004089.1:c.1400C= (LHCGR)	XP_016859578.1:p.Ala467=
XM_017004090.1:c.1019C= (LHCGR)	XP_016859579.1:p.Ala340=
NM_000233.4:c.1655C= (LHCGR) MANE Select	NP_000224.2:p.Ala552=
NM_001198593.2:c.3441+16462G= (STON1-GTF2A1L)	NP_001185522.1:n.3441+16462G=