Canonical Allele Identifier: CA1248601183

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688549G= , CM000664.2:g.48688549G=	GRCh38
NC_000002.11:g.48915688G= , CM000664.1:g.48915688G=	GRCh37
NC_000002.10:g.48769192G=	NCBI36
NG_008193.1:g.72193C=
NG_033050.1:g.163625G=
NG_008193.2:g.72193C=
NG_033050.2:g.163625G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000294954.12:c.1248C= (LHCGR) MANE Select	ENSP00000294954.6:p.Ala416=
ENST00000294954.11:c.1248C= (LHCGR)	ENSP00000294954.6:p.Ala416=
ENST00000401907.5:c.948-410C= (LHCGR)	ENSP00000385406.1:n.948-410C=
ENST00000402114.6:c.3441+16869G= (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16869G=
ENST00000403273.5:c.982C= (LHCGR)	ENSP00000385847.1:p.Leu328=
ENST00000405626.5:c.1167C= (LHCGR)	ENSP00000386033.1:p.Ala389=
ENST00000508440.1:c.276+16869G= (GTF2A1L)	ENSP00000421474.1:n.276+16869G=
ENST00000602369.3:c.*220+5675C=	ENSP00000473498.1:n.*220+5675C=
NM_000233.3:c.1248C= (LHCGR)	NP_000224.2:p.Ala416=
NM_001198593.1:c.3441+16869G= (STON1-GTF2A1L)	NP_001185522.1:n.3441+16869G=
XM_005264309.2:c.291C= (LHCGR)	XP_005264366.1:p.Ala97=
XM_006712015.2:c.318C= (LHCGR)	XP_006712078.1:p.Ala106=
XM_011532828.1:c.1173C= (LHCGR)	XP_011531130.1:p.Ala391=
XM_011532829.1:c.987C= (LHCGR)	XP_011531131.1:p.Ala329=
XM_011532830.1:c.906C= (LHCGR)	XP_011531132.1:p.Ala302=
XM_011532831.1:c.612C= (LHCGR)	XP_011531133.1:p.Ala204=
XM_011532832.1:c.318C= (LHCGR)	XP_011531134.1:p.Ala106=
XM_011532833.1:c.318C= (LHCGR)	XP_011531135.1:p.Ala106=
XM_011532834.1:c.291C= (LHCGR)	XP_011531136.1:p.Ala97=
XM_005264309.3:c.291C= (LHCGR)	XP_005264366.1:p.Ala97=
XM_006712015.3:c.318C= (LHCGR)	XP_006712078.1:p.Ala106=
XM_011532834.2:c.291C= (LHCGR)	XP_011531136.1:p.Ala97=
XM_017004089.1:c.993C= (LHCGR)	XP_016859578.1:p.Ala331=
XM_017004090.1:c.612C= (LHCGR)	XP_016859579.1:p.Ala204=
NM_000233.4:c.1248C= (LHCGR) MANE Select	NP_000224.2:p.Ala416=
NM_001198593.2:c.3441+16869G= (STON1-GTF2A1L)	NP_001185522.1:n.3441+16869G=