Canonical Allele Identifier: CA346746207
Gene: LHCGR HGNC NCBI
STON1-GTF2A1L HGNC NCBI
GTF2A1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.48688235G>C , CM000664.2:g.48688235G>C GRCh38
NC_000002.11:g.48915374G>C , CM000664.1:g.48915374G>C GRCh37
NC_000002.10:g.48768878G>C NCBI36
NG_008193.1:g.72507C>G
NG_033050.1:g.163311G>C
NG_008193.2:g.72507C>G
NG_033050.2:g.163311G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000294954.12:c.1562C>G (LHCGR) MANE Select ENSP00000294954.6:p.Thr521Ser
ENST00000294954.11:c.1562C>G (LHCGR) ENSP00000294954.6:p.Thr521Ser
ENST00000401907.5:c.948-96C>G (LHCGR) ENSP00000385406.1:n.948-96C>G
ENST00000402114.6:c.3441+16555G>C (STON1-GTF2A1L) ENSP00000385701.1:n.3441+16555G>C
ENST00000403273.5:c.*306C>G (LHCGR) ENSP00000385847.1:n.*306C>G
ENST00000405626.5:c.1481C>G (LHCGR) ENSP00000386033.1:p.Thr494Ser
ENST00000508440.1:c.276+16555G>C (GTF2A1L) ENSP00000421474.1:n.276+16555G>C
ENST00000602369.3:c.*220+5989C>G ENSP00000473498.1:n.*220+5989C>G
NM_000233.3:c.1562C>G (LHCGR) NP_000224.2:p.Thr521Ser
NM_001198593.1:c.3441+16555G>C (STON1-GTF2A1L) NP_001185522.1:n.3441+16555G>C
XM_005264309.2:c.605C>G (LHCGR) XP_005264366.1:p.Thr202Ser
XM_006712015.2:c.632C>G (LHCGR) XP_006712078.1:p.Thr211Ser
XM_011532828.1:c.1487C>G (LHCGR) XP_011531130.1:p.Thr496Ser
XM_011532829.1:c.1301C>G (LHCGR) XP_011531131.1:p.Thr434Ser
XM_011532830.1:c.1220C>G (LHCGR) XP_011531132.1:p.Thr407Ser
XM_011532831.1:c.926C>G (LHCGR) XP_011531133.1:p.Thr309Ser
XM_011532832.1:c.632C>G (LHCGR) XP_011531134.1:p.Thr211Ser
XM_011532833.1:c.632C>G (LHCGR) XP_011531135.1:p.Thr211Ser
XM_011532834.1:c.605C>G (LHCGR) XP_011531136.1:p.Thr202Ser
XM_005264309.3:c.605C>G (LHCGR) XP_005264366.1:p.Thr202Ser
XM_006712015.3:c.632C>G (LHCGR) XP_006712078.1:p.Thr211Ser
XM_011532834.2:c.605C>G (LHCGR) XP_011531136.1:p.Thr202Ser
XM_017004089.1:c.1307C>G (LHCGR) XP_016859578.1:p.Thr436Ser
XM_017004090.1:c.926C>G (LHCGR) XP_016859579.1:p.Thr309Ser
NM_000233.4:c.1562C>G (LHCGR) MANE Select NP_000224.2:p.Thr521Ser
NM_001198593.2:c.3441+16555G>C (STON1-GTF2A1L) NP_001185522.1:n.3441+16555G>C