Canonical Allele Identifier: CA346747197

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• MyVariant Identifiers: chr2:g.48915560A>T (hg19) ; chr2:g.48688421A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688421A>T , CM000664.2:g.48688421A>T	GRCh38
NC_000002.11:g.48915560A>T , CM000664.1:g.48915560A>T	GRCh37
NC_000002.10:g.48769064A>T	NCBI36
NG_008193.1:g.72321T>A
NG_033050.1:g.163497A>T
NG_008193.2:g.72321T>A
NG_033050.2:g.163497A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.1376T>A (LHCGR) MANE Select	ENSP00000294954.6:p.Val459Asp
ENST00000294954.11:c.1376T>A (LHCGR)	ENSP00000294954.6:p.Val459Asp
ENST00000401907.5:c.948-282T>A (LHCGR)	ENSP00000385406.1:n.948-282T>A
ENST00000402114.6:c.3441+16741A>T (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16741A>T
ENST00000403273.5:c.*120T>A (LHCGR)	ENSP00000385847.1:n.*120T>A
ENST00000405626.5:c.1295T>A (LHCGR)	ENSP00000386033.1:p.Val432Asp
ENST00000508440.1:c.276+16741A>T (GTF2A1L)	ENSP00000421474.1:n.276+16741A>T
ENST00000602369.3:c.*220+5803T>A	ENSP00000473498.1:n.*220+5803T>A
NM_000233.3:c.1376T>A (LHCGR)	NP_000224.2:p.Val459Asp
NM_001198593.1:c.3441+16741A>T (STON1-GTF2A1L)	NP_001185522.1:n.3441+16741A>T
XM_005264309.2:c.419T>A (LHCGR)	XP_005264366.1:p.Val140Asp
XM_006712015.2:c.446T>A (LHCGR)	XP_006712078.1:p.Val149Asp
XM_011532828.1:c.1301T>A (LHCGR)	XP_011531130.1:p.Val434Asp
XM_011532829.1:c.1115T>A (LHCGR)	XP_011531131.1:p.Val372Asp
XM_011532830.1:c.1034T>A (LHCGR)	XP_011531132.1:p.Val345Asp
XM_011532831.1:c.740T>A (LHCGR)	XP_011531133.1:p.Val247Asp
XM_011532832.1:c.446T>A (LHCGR)	XP_011531134.1:p.Val149Asp
XM_011532833.1:c.446T>A (LHCGR)	XP_011531135.1:p.Val149Asp
XM_011532834.1:c.419T>A (LHCGR)	XP_011531136.1:p.Val140Asp
XM_005264309.3:c.419T>A (LHCGR)	XP_005264366.1:p.Val140Asp
XM_006712015.3:c.446T>A (LHCGR)	XP_006712078.1:p.Val149Asp
XM_011532834.2:c.419T>A (LHCGR)	XP_011531136.1:p.Val140Asp
XM_017004089.1:c.1121T>A (LHCGR)	XP_016859578.1:p.Val374Asp
XM_017004090.1:c.740T>A (LHCGR)	XP_016859579.1:p.Val247Asp
NM_000233.4:c.1376T>A (LHCGR) MANE Select	NP_000224.2:p.Val459Asp
NM_001198593.2:c.3441+16741A>T (STON1-GTF2A1L)	NP_001185522.1:n.3441+16741A>T