Canonical Allele Identifier: CA2658994948

Gene: LHCGR STON1-GTF2A1L

Linked Data

• gnomAD v4: 2-48755411-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48755411T>C , CM000664.2:g.48755411T>C	GRCh38
NC_000002.11:g.48982550T>C , CM000664.1:g.48982550T>C	GRCh37
NC_000002.10:g.48836054T>C	NCBI36
NG_008193.1:g.5331A>G
NG_033050.1:g.230487T>C
NG_008193.2:g.5331A>G
NG_033050.2:g.230487T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.161+100A>G (LHCGR) MANE Select	ENSP00000294954.6:n.161+100A>G
ENST00000294954.11:c.161+100A>G (LHCGR)	ENSP00000294954.6:n.161+100A>G
ENST00000401907.5:c.161+100A>G (LHCGR)	ENSP00000385406.1:n.161+100A>G
ENST00000402114.6:c.3442-20869T>C (STON1-GTF2A1L)	ENSP00000385701.1:n.3442-20869T>C
ENST00000403273.5:c.161+100A>G (LHCGR)	ENSP00000385847.1:n.161+100A>G
ENST00000405626.5:c.161+100A>G (LHCGR)	ENSP00000386033.1:n.161+100A>G
ENST00000428232.2:c.59+100A>G (LHCGR)	ENSP00000403748.1:n.59+100A>G
ENST00000602369.3:c.161+100A>G	ENSP00000473498.1:n.161+100A>G
NM_000233.3:c.161+100A>G (LHCGR)	NP_000224.2:n.161+100A>G
NM_001198593.1:c.3442-20869T>C (STON1-GTF2A1L)	NP_001185522.1:n.3442-20869T>C
XM_011532828.1:c.161+100A>G (LHCGR)	XP_011531130.1:n.161+100A>G
XM_011532829.1:c.161+100A>G (LHCGR)	XP_011531131.1:n.161+100A>G
XM_011532830.1:c.161+100A>G (LHCGR)	XP_011531132.1:n.161+100A>G
NM_000233.4:c.161+100A>G (LHCGR) MANE Select	NP_000224.2:n.161+100A>G
NM_001198593.2:c.3442-20869T>C (STON1-GTF2A1L)	NP_001185522.1:n.3442-20869T>C