Canonical Allele Identifier: CA346746773

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• MyVariant Identifiers: chr2:g.48915457A>T (hg19) ; chr2:g.48688318A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688318A>T , CM000664.2:g.48688318A>T	GRCh38
NC_000002.11:g.48915457A>T , CM000664.1:g.48915457A>T	GRCh37
NC_000002.10:g.48768961A>T	NCBI36
NG_008193.1:g.72424T>A
NG_033050.1:g.163394A>T
NG_008193.2:g.72424T>A
NG_033050.2:g.163394A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.1479T>A (LHCGR) MANE Select	ENSP00000294954.6:p.Phe493Leu
ENST00000294954.11:c.1479T>A (LHCGR)	ENSP00000294954.6:p.Phe493Leu
ENST00000401907.5:c.948-179T>A (LHCGR)	ENSP00000385406.1:n.948-179T>A
ENST00000402114.6:c.3441+16638A>T (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16638A>T
ENST00000403273.5:c.*223T>A (LHCGR)	ENSP00000385847.1:n.*223T>A
ENST00000405626.5:c.1398T>A (LHCGR)	ENSP00000386033.1:p.Phe466Leu
ENST00000508440.1:c.276+16638A>T (GTF2A1L)	ENSP00000421474.1:n.276+16638A>T
ENST00000602369.3:c.*220+5906T>A	ENSP00000473498.1:n.*220+5906T>A
NM_000233.3:c.1479T>A (LHCGR)	NP_000224.2:p.Phe493Leu
NM_001198593.1:c.3441+16638A>T (STON1-GTF2A1L)	NP_001185522.1:n.3441+16638A>T
XM_005264309.2:c.522T>A (LHCGR)	XP_005264366.1:p.Phe174Leu
XM_006712015.2:c.549T>A (LHCGR)	XP_006712078.1:p.Phe183Leu
XM_011532828.1:c.1404T>A (LHCGR)	XP_011531130.1:p.Phe468Leu
XM_011532829.1:c.1218T>A (LHCGR)	XP_011531131.1:p.Phe406Leu
XM_011532830.1:c.1137T>A (LHCGR)	XP_011531132.1:p.Phe379Leu
XM_011532831.1:c.843T>A (LHCGR)	XP_011531133.1:p.Phe281Leu
XM_011532832.1:c.549T>A (LHCGR)	XP_011531134.1:p.Phe183Leu
XM_011532833.1:c.549T>A (LHCGR)	XP_011531135.1:p.Phe183Leu
XM_011532834.1:c.522T>A (LHCGR)	XP_011531136.1:p.Phe174Leu
XM_005264309.3:c.522T>A (LHCGR)	XP_005264366.1:p.Phe174Leu
XM_006712015.3:c.549T>A (LHCGR)	XP_006712078.1:p.Phe183Leu
XM_011532834.2:c.522T>A (LHCGR)	XP_011531136.1:p.Phe174Leu
XM_017004089.1:c.1224T>A (LHCGR)	XP_016859578.1:p.Phe408Leu
XM_017004090.1:c.843T>A (LHCGR)	XP_016859579.1:p.Phe281Leu
NM_000233.4:c.1479T>A (LHCGR) MANE Select	NP_000224.2:p.Phe493Leu
NM_001198593.2:c.3441+16638A>T (STON1-GTF2A1L)	NP_001185522.1:n.3441+16638A>T