Canonical Allele Identifier: CA1248601289

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688826C= , CM000664.2:g.48688826C=	GRCh38
NC_000002.11:g.48915965C= , CM000664.1:g.48915965C=	GRCh37
NC_000002.10:g.48769469C=	NCBI36
NG_008193.1:g.71916G=
NG_033050.1:g.163902C=
NG_008193.2:g.71916G=
NG_033050.2:g.163902C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.971G= (LHCGR) MANE Select	ENSP00000294954.6:p.Ser324=
ENST00000294954.11:c.971G= (LHCGR)	ENSP00000294954.6:p.Ser324=
ENST00000401907.5:c.948-687G= (LHCGR)	ENSP00000385406.1:n.948-687G=
ENST00000402114.6:c.3441+17146C= (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+17146C=
ENST00000403273.5:c.948-243G= (LHCGR)	ENSP00000385847.1:n.948-243G=
ENST00000405626.5:c.890G= (LHCGR)	ENSP00000386033.1:p.Ser297=
ENST00000508440.1:c.276+17146C= (GTF2A1L)	ENSP00000421474.1:n.276+17146C=
ENST00000602369.3:c.*220+5398G=	ENSP00000473498.1:n.*220+5398G=
NM_000233.3:c.971G= (LHCGR)	NP_000224.2:p.Ser324=
NM_001198593.1:c.3441+17146C= (STON1-GTF2A1L)	NP_001185522.1:n.3441+17146C=
XM_005264309.2:c.14G= (LHCGR)	XP_005264366.1:p.Ser5=
XM_006712015.2:c.41G= (LHCGR)	XP_006712078.1:p.Ser14=
XM_011532828.1:c.896G= (LHCGR)	XP_011531130.1:p.Ser299=
XM_011532829.1:c.710G= (LHCGR)	XP_011531131.1:p.Ser237=
XM_011532830.1:c.629G= (LHCGR)	XP_011531132.1:p.Ser210=
XM_011532831.1:c.335G= (LHCGR)	XP_011531133.1:p.Ser112=
XM_011532832.1:c.41G= (LHCGR)	XP_011531134.1:p.Ser14=
XM_011532833.1:c.41G= (LHCGR)	XP_011531135.1:p.Ser14=
XM_011532834.1:c.14G= (LHCGR)	XP_011531136.1:p.Ser5=
XM_005264309.3:c.14G= (LHCGR)	XP_005264366.1:p.Ser5=
XM_006712015.3:c.41G= (LHCGR)	XP_006712078.1:p.Ser14=
XM_011532834.2:c.14G= (LHCGR)	XP_011531136.1:p.Ser5=
XM_017004089.1:c.716G= (LHCGR)	XP_016859578.1:p.Ser239=
XM_017004090.1:c.335G= (LHCGR)	XP_016859579.1:p.Ser112=
NM_000233.4:c.971G= (LHCGR) MANE Select	NP_000224.2:p.Ser324=
NM_001198593.2:c.3441+17146C= (STON1-GTF2A1L)	NP_001185522.1:n.3441+17146C=