Canonical Allele Identifier: CA1248636659
Gene: LHCGR HGNC NCBI
STON1-GTF2A1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.48755410C= , CM000664.2:g.48755410C= GRCh38
NC_000002.11:g.48982549C= , CM000664.1:g.48982549C= GRCh37
NC_000002.10:g.48836053C= NCBI36
NG_008193.1:g.5332G=
NG_033050.1:g.230486C=
NG_008193.2:g.5332G=
NG_033050.2:g.230486C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000294954.12:c.161+101G= (LHCGR) MANE Select ENSP00000294954.6:n.161+101G=
ENST00000294954.11:c.161+101G= (LHCGR) ENSP00000294954.6:n.161+101G=
ENST00000401907.5:c.161+101G= (LHCGR) ENSP00000385406.1:n.161+101G=
ENST00000402114.6:c.3442-20870C= (STON1-GTF2A1L) ENSP00000385701.1:n.3442-20870C=
ENST00000403273.5:c.161+101G= (LHCGR) ENSP00000385847.1:n.161+101G=
ENST00000405626.5:c.161+101G= (LHCGR) ENSP00000386033.1:n.161+101G=
ENST00000428232.2:c.59+101G= (LHCGR) ENSP00000403748.1:n.59+101G=
ENST00000602369.3:c.161+101G= ENSP00000473498.1:n.161+101G=
NM_000233.3:c.161+101G= (LHCGR) NP_000224.2:n.161+101G=
NM_001198593.1:c.3442-20870C= (STON1-GTF2A1L) NP_001185522.1:n.3442-20870C=
XM_011532828.1:c.161+101G= (LHCGR) XP_011531130.1:n.161+101G=
XM_011532829.1:c.161+101G= (LHCGR) XP_011531131.1:n.161+101G=
XM_011532830.1:c.161+101G= (LHCGR) XP_011531132.1:n.161+101G=
NM_000233.4:c.161+101G= (LHCGR) MANE Select NP_000224.2:n.161+101G=
NM_001198593.2:c.3442-20870C= (STON1-GTF2A1L) NP_001185522.1:n.3442-20870C=