Canonical Allele Identifier: CA346744301

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• dbSNP Id: rs547124114
• gnomAD v2: 2-48915105-A-G
• gnomAD v4: 2-48687966-A-G
• MyVariant Identifiers: chr2:g.48915105A>G (hg19) ; chr2:g.48687966A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48687966A>G , CM000664.2:g.48687966A>G	GRCh38
NC_000002.11:g.48915105A>G , CM000664.1:g.48915105A>G	GRCh37
NC_000002.10:g.48768609A>G	NCBI36
NG_008193.1:g.72776T>C
NG_033050.1:g.163042A>G
NG_008193.2:g.72776T>C
NG_033050.2:g.163042A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.1831T>C (LHCGR) MANE Select	ENSP00000294954.6:p.Phe611Leu
ENST00000294954.11:c.1831T>C (LHCGR)	ENSP00000294954.6:p.Phe611Leu
ENST00000401907.5:c.*143T>C (LHCGR)	ENSP00000385406.1:n.*143T>C
ENST00000402114.6:c.3441+16286A>G (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16286A>G
ENST00000403273.5:c.*575T>C (LHCGR)	ENSP00000385847.1:n.*575T>C
ENST00000405626.5:c.1750T>C (LHCGR)	ENSP00000386033.1:p.Phe584Leu
ENST00000508440.1:c.276+16286A>G (GTF2A1L)	ENSP00000421474.1:n.276+16286A>G
ENST00000602369.3:c.*220+6258T>C	ENSP00000473498.1:n.*220+6258T>C
NM_000233.3:c.1831T>C (LHCGR)	NP_000224.2:p.Phe611Leu
NM_001198593.1:c.3441+16286A>G (STON1-GTF2A1L)	NP_001185522.1:n.3441+16286A>G
XM_005264309.2:c.874T>C (LHCGR)	XP_005264366.1:p.Phe292Leu
XM_006712015.2:c.901T>C (LHCGR)	XP_006712078.1:p.Phe301Leu
XM_011532828.1:c.1756T>C (LHCGR)	XP_011531130.1:p.Phe586Leu
XM_011532829.1:c.1570T>C (LHCGR)	XP_011531131.1:p.Phe524Leu
XM_011532830.1:c.1489T>C (LHCGR)	XP_011531132.1:p.Phe497Leu
XM_011532831.1:c.1195T>C (LHCGR)	XP_011531133.1:p.Phe399Leu
XM_011532832.1:c.901T>C (LHCGR)	XP_011531134.1:p.Phe301Leu
XM_011532833.1:c.901T>C (LHCGR)	XP_011531135.1:p.Phe301Leu
XM_011532834.1:c.874T>C (LHCGR)	XP_011531136.1:p.Phe292Leu
XM_005264309.3:c.874T>C (LHCGR)	XP_005264366.1:p.Phe292Leu
XM_006712015.3:c.901T>C (LHCGR)	XP_006712078.1:p.Phe301Leu
XM_011532834.2:c.874T>C (LHCGR)	XP_011531136.1:p.Phe292Leu
XM_017004089.1:c.1576T>C (LHCGR)	XP_016859578.1:p.Phe526Leu
XM_017004090.1:c.1195T>C (LHCGR)	XP_016859579.1:p.Phe399Leu
NM_000233.4:c.1831T>C (LHCGR) MANE Select	NP_000224.2:p.Phe611Leu
NM_001198593.2:c.3441+16286A>G (STON1-GTF2A1L)	NP_001185522.1:n.3441+16286A>G