Canonical Allele Identifier: CA346745510

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• MyVariant Identifiers: chr2:g.48915282C>A (hg19) ; chr2:g.48688143C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688143C>A , CM000664.2:g.48688143C>A	GRCh38
NC_000002.11:g.48915282C>A , CM000664.1:g.48915282C>A	GRCh37
NC_000002.10:g.48768786C>A	NCBI36
NG_008193.1:g.72599G>T
NG_033050.1:g.163219C>A
NG_008193.2:g.72599G>T
NG_033050.2:g.163219C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.1654G>T (LHCGR) MANE Select	ENSP00000294954.6:p.Ala552Ser
ENST00000294954.11:c.1654G>T (LHCGR)	ENSP00000294954.6:p.Ala552Ser
ENST00000401907.5:c.948-4G>T (LHCGR)	ENSP00000385406.1:n.948-4G>T
ENST00000402114.6:c.3441+16463C>A (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16463C>A
ENST00000403273.5:c.*398G>T (LHCGR)	ENSP00000385847.1:n.*398G>T
ENST00000405626.5:c.1573G>T (LHCGR)	ENSP00000386033.1:p.Ala525Ser
ENST00000508440.1:c.276+16463C>A (GTF2A1L)	ENSP00000421474.1:n.276+16463C>A
ENST00000602369.3:c.*220+6081G>T	ENSP00000473498.1:n.*220+6081G>T
NM_000233.3:c.1654G>T (LHCGR)	NP_000224.2:p.Ala552Ser
NM_001198593.1:c.3441+16463C>A (STON1-GTF2A1L)	NP_001185522.1:n.3441+16463C>A
XM_005264309.2:c.697G>T (LHCGR)	XP_005264366.1:p.Ala233Ser
XM_006712015.2:c.724G>T (LHCGR)	XP_006712078.1:p.Ala242Ser
XM_011532828.1:c.1579G>T (LHCGR)	XP_011531130.1:p.Ala527Ser
XM_011532829.1:c.1393G>T (LHCGR)	XP_011531131.1:p.Ala465Ser
XM_011532830.1:c.1312G>T (LHCGR)	XP_011531132.1:p.Ala438Ser
XM_011532831.1:c.1018G>T (LHCGR)	XP_011531133.1:p.Ala340Ser
XM_011532832.1:c.724G>T (LHCGR)	XP_011531134.1:p.Ala242Ser
XM_011532833.1:c.724G>T (LHCGR)	XP_011531135.1:p.Ala242Ser
XM_011532834.1:c.697G>T (LHCGR)	XP_011531136.1:p.Ala233Ser
XM_005264309.3:c.697G>T (LHCGR)	XP_005264366.1:p.Ala233Ser
XM_006712015.3:c.724G>T (LHCGR)	XP_006712078.1:p.Ala242Ser
XM_011532834.2:c.697G>T (LHCGR)	XP_011531136.1:p.Ala233Ser
XM_017004089.1:c.1399G>T (LHCGR)	XP_016859578.1:p.Ala467Ser
XM_017004090.1:c.1018G>T (LHCGR)	XP_016859579.1:p.Ala340Ser
NM_000233.4:c.1654G>T (LHCGR) MANE Select	NP_000224.2:p.Ala552Ser
NM_001198593.2:c.3441+16463C>A (STON1-GTF2A1L)	NP_001185522.1:n.3441+16463C>A