Canonical Allele Identifier: CA1248636849

Gene: LHCGR STON1-GTF2A1L

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48755703G= , CM000664.2:g.48755703G=	GRCh38
NC_000002.11:g.48982842G= , CM000664.1:g.48982842G=	GRCh37
NC_000002.10:g.48836346G=	NCBI36
NG_008193.1:g.5039C=
NG_033050.1:g.230779G=
NG_008193.2:g.5039C=
NG_033050.2:g.230779G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.-32C= (LHCGR) MANE Select	ENSP00000294954.6:n.-32C=
ENST00000401907.5:c.-32C= (LHCGR)	ENSP00000385406.1:n.-32C=
ENST00000402114.6:c.3442-20577G= (STON1-GTF2A1L)	ENSP00000385701.1:n.3442-20577G=
ENST00000403273.5:c.-32C= (LHCGR)	ENSP00000385847.1:n.-32C=
ENST00000602369.3:c.-32C=	ENSP00000473498.1:n.-32C=
NM_000233.3:c.-32C= (LHCGR)	NP_000224.2:n.-32C=
NM_001198593.1:c.3442-20577G= (STON1-GTF2A1L)	NP_001185522.1:n.3442-20577G=
XM_011532828.1:c.-32C= (LHCGR)	XP_011531130.1:n.-32C=
XM_011532829.1:c.-32C= (LHCGR)	XP_011531131.1:n.-32C=
XM_011532830.1:c.-32C= (LHCGR)	XP_011531132.1:n.-32C=
NM_000233.4:c.-32C= (LHCGR) MANE Select	NP_000224.2:n.-32C=
NM_001198593.2:c.3442-20577G= (STON1-GTF2A1L)	NP_001185522.1:n.3442-20577G=