Canonical Allele Identifier: CA346746721
Gene: LHCGR HGNC NCBI
STON1-GTF2A1L HGNC NCBI
GTF2A1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.48688306A>C , CM000664.2:g.48688306A>C GRCh38
NC_000002.11:g.48915445A>C , CM000664.1:g.48915445A>C GRCh37
NC_000002.10:g.48768949A>C NCBI36
NG_008193.1:g.72436T>G
NG_033050.1:g.163382A>C
NG_008193.2:g.72436T>G
NG_033050.2:g.163382A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000294954.12:c.1491T>G (LHCGR) MANE Select ENSP00000294954.6:p.Ile497Met
ENST00000294954.11:c.1491T>G (LHCGR) ENSP00000294954.6:p.Ile497Met
ENST00000401907.5:c.948-167T>G (LHCGR) ENSP00000385406.1:n.948-167T>G
ENST00000402114.6:c.3441+16626A>C (STON1-GTF2A1L) ENSP00000385701.1:n.3441+16626A>C
ENST00000403273.5:c.*235T>G (LHCGR) ENSP00000385847.1:n.*235T>G
ENST00000405626.5:c.1410T>G (LHCGR) ENSP00000386033.1:p.Ile470Met
ENST00000508440.1:c.276+16626A>C (GTF2A1L) ENSP00000421474.1:n.276+16626A>C
ENST00000602369.3:c.*220+5918T>G ENSP00000473498.1:n.*220+5918T>G
NM_000233.3:c.1491T>G (LHCGR) NP_000224.2:p.Ile497Met
NM_001198593.1:c.3441+16626A>C (STON1-GTF2A1L) NP_001185522.1:n.3441+16626A>C
XM_005264309.2:c.534T>G (LHCGR) XP_005264366.1:p.Ile178Met
XM_006712015.2:c.561T>G (LHCGR) XP_006712078.1:p.Ile187Met
XM_011532828.1:c.1416T>G (LHCGR) XP_011531130.1:p.Ile472Met
XM_011532829.1:c.1230T>G (LHCGR) XP_011531131.1:p.Ile410Met
XM_011532830.1:c.1149T>G (LHCGR) XP_011531132.1:p.Ile383Met
XM_011532831.1:c.855T>G (LHCGR) XP_011531133.1:p.Ile285Met
XM_011532832.1:c.561T>G (LHCGR) XP_011531134.1:p.Ile187Met
XM_011532833.1:c.561T>G (LHCGR) XP_011531135.1:p.Ile187Met
XM_011532834.1:c.534T>G (LHCGR) XP_011531136.1:p.Ile178Met
XM_005264309.3:c.534T>G (LHCGR) XP_005264366.1:p.Ile178Met
XM_006712015.3:c.561T>G (LHCGR) XP_006712078.1:p.Ile187Met
XM_011532834.2:c.534T>G (LHCGR) XP_011531136.1:p.Ile178Met
XM_017004089.1:c.1236T>G (LHCGR) XP_016859578.1:p.Ile412Met
XM_017004090.1:c.855T>G (LHCGR) XP_016859579.1:p.Ile285Met
NM_000233.4:c.1491T>G (LHCGR) MANE Select NP_000224.2:p.Ile497Met
NM_001198593.2:c.3441+16626A>C (STON1-GTF2A1L) NP_001185522.1:n.3441+16626A>C