Canonical Allele Identifier: CA1248601032

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688207G= , CM000664.2:g.48688207G=	GRCh38
NC_000002.11:g.48915346G= , CM000664.1:g.48915346G=	GRCh37
NC_000002.10:g.48768850G=	NCBI36
NG_008193.1:g.72535C=
NG_033050.1:g.163283G=
NG_008193.2:g.72535C=
NG_033050.2:g.163283G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.1590C= (LHCGR) MANE Select	ENSP00000294954.6:p.Thr530=
ENST00000294954.11:c.1590C= (LHCGR)	ENSP00000294954.6:p.Thr530=
ENST00000401907.5:c.948-68C= (LHCGR)	ENSP00000385406.1:n.948-68C=
ENST00000402114.6:c.3441+16527G= (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16527G=
ENST00000403273.5:c.*334C= (LHCGR)	ENSP00000385847.1:n.*334C=
ENST00000405626.5:c.1509C= (LHCGR)	ENSP00000386033.1:p.Thr503=
ENST00000508440.1:c.276+16527G= (GTF2A1L)	ENSP00000421474.1:n.276+16527G=
ENST00000602369.3:c.*220+6017C=	ENSP00000473498.1:n.*220+6017C=
NM_000233.3:c.1590C= (LHCGR)	NP_000224.2:p.Thr530=
NM_001198593.1:c.3441+16527G= (STON1-GTF2A1L)	NP_001185522.1:n.3441+16527G=
XM_005264309.2:c.633C= (LHCGR)	XP_005264366.1:p.Thr211=
XM_006712015.2:c.660C= (LHCGR)	XP_006712078.1:p.Thr220=
XM_011532828.1:c.1515C= (LHCGR)	XP_011531130.1:p.Thr505=
XM_011532829.1:c.1329C= (LHCGR)	XP_011531131.1:p.Thr443=
XM_011532830.1:c.1248C= (LHCGR)	XP_011531132.1:p.Thr416=
XM_011532831.1:c.954C= (LHCGR)	XP_011531133.1:p.Thr318=
XM_011532832.1:c.660C= (LHCGR)	XP_011531134.1:p.Thr220=
XM_011532833.1:c.660C= (LHCGR)	XP_011531135.1:p.Thr220=
XM_011532834.1:c.633C= (LHCGR)	XP_011531136.1:p.Thr211=
XM_005264309.3:c.633C= (LHCGR)	XP_005264366.1:p.Thr211=
XM_006712015.3:c.660C= (LHCGR)	XP_006712078.1:p.Thr220=
XM_011532834.2:c.633C= (LHCGR)	XP_011531136.1:p.Thr211=
XM_017004089.1:c.1335C= (LHCGR)	XP_016859578.1:p.Thr445=
XM_017004090.1:c.954C= (LHCGR)	XP_016859579.1:p.Thr318=
NM_000233.4:c.1590C= (LHCGR) MANE Select	NP_000224.2:p.Thr530=
NM_001198593.2:c.3441+16527G= (STON1-GTF2A1L)	NP_001185522.1:n.3441+16527G=