Canonical Allele Identifier: CA1248600989
Gene: LHCGR HGNC NCBI
STON1-GTF2A1L HGNC NCBI
GTF2A1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.48688098_48688099delinsTC , CM000664.2:g.48688098_48688099delinsTC GRCh38
NC_000002.11:g.48915237_48915238delinsTC , CM000664.1:g.48915237_48915238delinsTC GRCh37
NC_000002.10:g.48768741_48768742delinsTC NCBI36
NG_008193.1:g.72643_72644delinsGA
NG_033050.1:g.163174_163175delinsTC
NG_008193.2:g.72643_72644delinsGA
NG_033050.2:g.163174_163175delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000294954.12:c.1698_1699delinsGA (LHCGR) MANE Select ENSP00000294954.6:p.Lys566=
ENST00000294954.11:c.1698_1699delinsGA (LHCGR) ENSP00000294954.6:p.Lys566=
ENST00000401907.5:c.*10_*11delinsGA (LHCGR) ENSP00000385406.1:n.*10_*11delinsGA
ENST00000402114.6:c.3441+16418_3441+16419delinsTC (STON1-GTF2A1L) ENSP00000385701.1:n.3441+16418_3441+16419delinsTC
ENST00000403273.5:c.*442_*443delinsGA (LHCGR) ENSP00000385847.1:n.*442_*443delinsGA
ENST00000405626.5:c.1617_1618delinsGA (LHCGR) ENSP00000386033.1:p.Lys539=
ENST00000508440.1:c.276+16418_276+16419delinsTC (GTF2A1L) ENSP00000421474.1:n.276+16418_276+16419delinsTC
ENST00000602369.3:c.*220+6125_*220+6126delinsGA ENSP00000473498.1:n.*220+6125_*220+6126delinsGA
NM_000233.3:c.1698_1699delinsGA (LHCGR) NP_000224.2:p.Lys566=
NM_001198593.1:c.3441+16418_3441+16419delinsTC (STON1-GTF2A1L) NP_001185522.1:n.3441+16418_3441+16419delinsTC
XM_005264309.2:c.741_742delinsGA (LHCGR) XP_005264366.1:p.Lys247=
XM_006712015.2:c.768_769delinsGA (LHCGR) XP_006712078.1:p.Lys256=
XM_011532828.1:c.1623_1624delinsGA (LHCGR) XP_011531130.1:p.Lys541=
XM_011532829.1:c.1437_1438delinsGA (LHCGR) XP_011531131.1:p.Lys479=
XM_011532830.1:c.1356_1357delinsGA (LHCGR) XP_011531132.1:p.Lys452=
XM_011532831.1:c.1062_1063delinsGA (LHCGR) XP_011531133.1:p.Lys354=
XM_011532832.1:c.768_769delinsGA (LHCGR) XP_011531134.1:p.Lys256=
XM_011532833.1:c.768_769delinsGA (LHCGR) XP_011531135.1:p.Lys256=
XM_011532834.1:c.741_742delinsGA (LHCGR) XP_011531136.1:p.Lys247=
XM_005264309.3:c.741_742delinsGA (LHCGR) XP_005264366.1:p.Lys247=
XM_006712015.3:c.768_769delinsGA (LHCGR) XP_006712078.1:p.Lys256=
XM_011532834.2:c.741_742delinsGA (LHCGR) XP_011531136.1:p.Lys247=
XM_017004089.1:c.1443_1444delinsGA (LHCGR) XP_016859578.1:p.Lys481=
XM_017004090.1:c.1062_1063delinsGA (LHCGR) XP_016859579.1:p.Lys354=
NM_000233.4:c.1698_1699delinsGA (LHCGR) MANE Select NP_000224.2:p.Lys566=
NM_001198593.2:c.3441+16418_3441+16419delinsTC (STON1-GTF2A1L) NP_001185522.1:n.3441+16418_3441+16419delinsTC