Canonical Allele Identifier: CA346749071

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• MyVariant Identifiers: chr2:g.48915777T>G (hg19) ; chr2:g.48688638T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688638T>G , CM000664.2:g.48688638T>G	GRCh38
NC_000002.11:g.48915777T>G , CM000664.1:g.48915777T>G	GRCh37
NC_000002.10:g.48769281T>G	NCBI36
NG_008193.1:g.72104A>C
NG_033050.1:g.163714T>G
NG_008193.2:g.72104A>C
NG_033050.2:g.163714T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000294954.12:c.1159A>C (LHCGR) MANE Select	ENSP00000294954.6:p.Ser387Arg
ENST00000294954.11:c.1159A>C (LHCGR)	ENSP00000294954.6:p.Ser387Arg
ENST00000401907.5:c.948-499A>C (LHCGR)	ENSP00000385406.1:n.948-499A>C
ENST00000402114.6:c.3441+16958T>G (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16958T>G
ENST00000403273.5:c.948-55A>C (LHCGR)	ENSP00000385847.1:n.948-55A>C
ENST00000405626.5:c.1078A>C (LHCGR)	ENSP00000386033.1:p.Ser360Arg
ENST00000508440.1:c.276+16958T>G (GTF2A1L)	ENSP00000421474.1:n.276+16958T>G
ENST00000602369.3:c.*220+5586A>C	ENSP00000473498.1:n.*220+5586A>C
NM_000233.3:c.1159A>C (LHCGR)	NP_000224.2:p.Ser387Arg
NM_001198593.1:c.3441+16958T>G (STON1-GTF2A1L)	NP_001185522.1:n.3441+16958T>G
XM_005264309.2:c.202A>C (LHCGR)	XP_005264366.1:p.Ser68Arg
XM_006712015.2:c.229A>C (LHCGR)	XP_006712078.1:p.Ser77Arg
XM_011532828.1:c.1084A>C (LHCGR)	XP_011531130.1:p.Ser362Arg
XM_011532829.1:c.898A>C (LHCGR)	XP_011531131.1:p.Ser300Arg
XM_011532830.1:c.817A>C (LHCGR)	XP_011531132.1:p.Ser273Arg
XM_011532831.1:c.523A>C (LHCGR)	XP_011531133.1:p.Ser175Arg
XM_011532832.1:c.229A>C (LHCGR)	XP_011531134.1:p.Ser77Arg
XM_011532833.1:c.229A>C (LHCGR)	XP_011531135.1:p.Ser77Arg
XM_011532834.1:c.202A>C (LHCGR)	XP_011531136.1:p.Ser68Arg
XM_005264309.3:c.202A>C (LHCGR)	XP_005264366.1:p.Ser68Arg
XM_006712015.3:c.229A>C (LHCGR)	XP_006712078.1:p.Ser77Arg
XM_011532834.2:c.202A>C (LHCGR)	XP_011531136.1:p.Ser68Arg
XM_017004089.1:c.904A>C (LHCGR)	XP_016859578.1:p.Ser302Arg
XM_017004090.1:c.523A>C (LHCGR)	XP_016859579.1:p.Ser175Arg
NM_000233.4:c.1159A>C (LHCGR) MANE Select	NP_000224.2:p.Ser387Arg
NM_001198593.2:c.3441+16958T>G (STON1-GTF2A1L)	NP_001185522.1:n.3441+16958T>G