Canonical Allele Identifier: CA1248636731
Gene: LHCGR HGNC NCBI
STON1-GTF2A1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.48755529G= , CM000664.2:g.48755529G= GRCh38
NC_000002.11:g.48982668G= , CM000664.1:g.48982668G= GRCh37
NC_000002.10:g.48836172G= NCBI36
NG_008193.1:g.5213C=
NG_033050.1:g.230605G=
NG_008193.2:g.5213C=
NG_033050.2:g.230605G=

Transcript Alleles

HGVS Amino-acid change
ENST00000294954.12:c.143C= (LHCGR) MANE Select ENSP00000294954.6:p.Thr48=
ENST00000294954.11:c.143C= (LHCGR) ENSP00000294954.6:p.Thr48=
ENST00000401907.5:c.143C= (LHCGR) ENSP00000385406.1:p.Thr48=
ENST00000402114.6:c.3442-20751G= (STON1-GTF2A1L) ENSP00000385701.1:n.3442-20751G=
ENST00000403273.5:c.143C= (LHCGR) ENSP00000385847.1:p.Thr48=
ENST00000405626.5:c.143C= (LHCGR) ENSP00000386033.1:p.Thr48=
ENST00000428232.2:c.41C= (LHCGR) ENSP00000403748.1:p.Thr14=
ENST00000602369.3:c.143C= ENSP00000473498.1:p.Thr48=
NM_000233.3:c.143C= (LHCGR) NP_000224.2:p.Thr48=
NM_001198593.1:c.3442-20751G= (STON1-GTF2A1L) NP_001185522.1:n.3442-20751G=
XM_011532828.1:c.143C= (LHCGR) XP_011531130.1:p.Thr48=
XM_011532829.1:c.143C= (LHCGR) XP_011531131.1:p.Thr48=
XM_011532830.1:c.143C= (LHCGR) XP_011531132.1:p.Thr48=
NM_000233.4:c.143C= (LHCGR) MANE Select NP_000224.2:p.Thr48=
NM_001198593.2:c.3442-20751G= (STON1-GTF2A1L) NP_001185522.1:n.3442-20751G=