Canonical Allele Identifier: CA1248601133

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688437C= , CM000664.2:g.48688437C=	GRCh38
NC_000002.11:g.48915576C= , CM000664.1:g.48915576C=	GRCh37
NC_000002.10:g.48769080C=	NCBI36
NG_008193.1:g.72305G=
NG_033050.1:g.163513C=
NG_008193.2:g.72305G=
NG_033050.2:g.163513C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000294954.12:c.1360G= (LHCGR) MANE Select	ENSP00000294954.6:p.Val454=
ENST00000294954.11:c.1360G= (LHCGR)	ENSP00000294954.6:p.Val454=
ENST00000401907.5:c.948-298G= (LHCGR)	ENSP00000385406.1:n.948-298G=
ENST00000402114.6:c.3441+16757C= (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16757C=
ENST00000403273.5:c.*104G= (LHCGR)	ENSP00000385847.1:n.*104G=
ENST00000405626.5:c.1279G= (LHCGR)	ENSP00000386033.1:p.Val427=
ENST00000508440.1:c.276+16757C= (GTF2A1L)	ENSP00000421474.1:n.276+16757C=
ENST00000602369.3:c.*220+5787G=	ENSP00000473498.1:n.*220+5787G=
NM_000233.3:c.1360G= (LHCGR)	NP_000224.2:p.Val454=
NM_001198593.1:c.3441+16757C= (STON1-GTF2A1L)	NP_001185522.1:n.3441+16757C=
XM_005264309.2:c.403G= (LHCGR)	XP_005264366.1:p.Val135=
XM_006712015.2:c.430G= (LHCGR)	XP_006712078.1:p.Val144=
XM_011532828.1:c.1285G= (LHCGR)	XP_011531130.1:p.Val429=
XM_011532829.1:c.1099G= (LHCGR)	XP_011531131.1:p.Val367=
XM_011532830.1:c.1018G= (LHCGR)	XP_011531132.1:p.Val340=
XM_011532831.1:c.724G= (LHCGR)	XP_011531133.1:p.Val242=
XM_011532832.1:c.430G= (LHCGR)	XP_011531134.1:p.Val144=
XM_011532833.1:c.430G= (LHCGR)	XP_011531135.1:p.Val144=
XM_011532834.1:c.403G= (LHCGR)	XP_011531136.1:p.Val135=
XM_005264309.3:c.403G= (LHCGR)	XP_005264366.1:p.Val135=
XM_006712015.3:c.430G= (LHCGR)	XP_006712078.1:p.Val144=
XM_011532834.2:c.403G= (LHCGR)	XP_011531136.1:p.Val135=
XM_017004089.1:c.1105G= (LHCGR)	XP_016859578.1:p.Val369=
XM_017004090.1:c.724G= (LHCGR)	XP_016859579.1:p.Val242=
NM_000233.4:c.1360G= (LHCGR) MANE Select	NP_000224.2:p.Val454=
NM_001198593.2:c.3441+16757C= (STON1-GTF2A1L)	NP_001185522.1:n.3441+16757C=