Canonical Allele Identifier: CA426124885
Gene: LHCGR HGNC NCBI
STON1-GTF2A1L HGNC NCBI
GTF2A1L HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.48915142A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.48688003A>G , CM000664.2:g.48688003A>G GRCh38
NC_000002.11:g.48915142A>G , CM000664.1:g.48915142A>G GRCh37
NC_000002.10:g.48768646A>G NCBI36
NG_008193.1:g.72739T>C
NG_033050.1:g.163079A>G
NG_008193.2:g.72739T>C
NG_033050.2:g.163079A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000294954.12:c.1794T>C (LHCGR) MANE Select ENSP00000294954.6:p.Leu598=
ENST00000294954.11:c.1794T>C (LHCGR) ENSP00000294954.6:p.Leu598=
ENST00000401907.5:c.*106T>C (LHCGR) ENSP00000385406.1:n.*106T>C
ENST00000402114.6:c.3441+16323A>G (STON1-GTF2A1L) ENSP00000385701.1:n.3441+16323A>G
ENST00000403273.5:c.*538T>C (LHCGR) ENSP00000385847.1:n.*538T>C
ENST00000405626.5:c.1713T>C (LHCGR) ENSP00000386033.1:p.Leu571=
ENST00000508440.1:c.276+16323A>G (GTF2A1L) ENSP00000421474.1:n.276+16323A>G
ENST00000602369.3:c.*220+6221T>C ENSP00000473498.1:n.*220+6221T>C
NM_000233.3:c.1794T>C (LHCGR) NP_000224.2:p.Leu598=
NM_001198593.1:c.3441+16323A>G (STON1-GTF2A1L) NP_001185522.1:n.3441+16323A>G
XM_005264309.2:c.837T>C (LHCGR) XP_005264366.1:p.Leu279=
XM_006712015.2:c.864T>C (LHCGR) XP_006712078.1:p.Leu288=
XM_011532828.1:c.1719T>C (LHCGR) XP_011531130.1:p.Leu573=
XM_011532829.1:c.1533T>C (LHCGR) XP_011531131.1:p.Leu511=
XM_011532830.1:c.1452T>C (LHCGR) XP_011531132.1:p.Leu484=
XM_011532831.1:c.1158T>C (LHCGR) XP_011531133.1:p.Leu386=
XM_011532832.1:c.864T>C (LHCGR) XP_011531134.1:p.Leu288=
XM_011532833.1:c.864T>C (LHCGR) XP_011531135.1:p.Leu288=
XM_011532834.1:c.837T>C (LHCGR) XP_011531136.1:p.Leu279=
XM_005264309.3:c.837T>C (LHCGR) XP_005264366.1:p.Leu279=
XM_006712015.3:c.864T>C (LHCGR) XP_006712078.1:p.Leu288=
XM_011532834.2:c.837T>C (LHCGR) XP_011531136.1:p.Leu279=
XM_017004089.1:c.1539T>C (LHCGR) XP_016859578.1:p.Leu513=
XM_017004090.1:c.1158T>C (LHCGR) XP_016859579.1:p.Leu386=
NM_000233.4:c.1794T>C (LHCGR) MANE Select NP_000224.2:p.Leu598=
NM_001198593.2:c.3441+16323A>G (STON1-GTF2A1L) NP_001185522.1:n.3441+16323A>G