Canonical Allele Identifier: CA346745190

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• ClinVar Variation Id: 1458111
• ClinVar RCV Id: RCV001949425
• dbSNP Id: rs121912540
• MyVariant Identifiers: chr2:g.48915245T>A (hg19) ; chr2:g.48688106T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688106T>A , CM000664.2:g.48688106T>A	GRCh38
NC_000002.11:g.48915245T>A , CM000664.1:g.48915245T>A	GRCh37
NC_000002.10:g.48768749T>A	NCBI36
NG_008193.1:g.72636A>T
NG_033050.1:g.163182T>A
NG_008193.2:g.72636A>T
NG_033050.2:g.163182T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000294954.12:c.1691A>T (LHCGR) MANE Select	ENSP00000294954.6:p.Asp564Val
ENST00000294954.11:c.1691A>T (LHCGR)	ENSP00000294954.6:p.Asp564Val
ENST00000401907.5:c.*3A>T (LHCGR)	ENSP00000385406.1:n.*3A>T
ENST00000402114.6:c.3441+16426T>A (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16426T>A
ENST00000403273.5:c.*435A>T (LHCGR)	ENSP00000385847.1:n.*435A>T
ENST00000405626.5:c.1610A>T (LHCGR)	ENSP00000386033.1:p.Asp537Val
ENST00000508440.1:c.276+16426T>A (GTF2A1L)	ENSP00000421474.1:n.276+16426T>A
ENST00000602369.3:c.*220+6118A>T	ENSP00000473498.1:n.*220+6118A>T
NM_000233.3:c.1691A>T (LHCGR)	NP_000224.2:p.Asp564Val
NM_001198593.1:c.3441+16426T>A (STON1-GTF2A1L)	NP_001185522.1:n.3441+16426T>A
XM_005264309.2:c.734A>T (LHCGR)	XP_005264366.1:p.Asp245Val
XM_006712015.2:c.761A>T (LHCGR)	XP_006712078.1:p.Asp254Val
XM_011532828.1:c.1616A>T (LHCGR)	XP_011531130.1:p.Asp539Val
XM_011532829.1:c.1430A>T (LHCGR)	XP_011531131.1:p.Asp477Val
XM_011532830.1:c.1349A>T (LHCGR)	XP_011531132.1:p.Asp450Val
XM_011532831.1:c.1055A>T (LHCGR)	XP_011531133.1:p.Asp352Val
XM_011532832.1:c.761A>T (LHCGR)	XP_011531134.1:p.Asp254Val
XM_011532833.1:c.761A>T (LHCGR)	XP_011531135.1:p.Asp254Val
XM_011532834.1:c.734A>T (LHCGR)	XP_011531136.1:p.Asp245Val
XM_005264309.3:c.734A>T (LHCGR)	XP_005264366.1:p.Asp245Val
XM_006712015.3:c.761A>T (LHCGR)	XP_006712078.1:p.Asp254Val
XM_011532834.2:c.734A>T (LHCGR)	XP_011531136.1:p.Asp245Val
XM_017004089.1:c.1436A>T (LHCGR)	XP_016859578.1:p.Asp479Val
XM_017004090.1:c.1055A>T (LHCGR)	XP_016859579.1:p.Asp352Val
NM_000233.4:c.1691A>T (LHCGR) MANE Select	NP_000224.2:p.Asp564Val
NM_001198593.2:c.3441+16426T>A (STON1-GTF2A1L)	NP_001185522.1:n.3441+16426T>A