Canonical Allele Identifier: CA346815620

Gene: LHCGR STON1-GTF2A1L

Linked Data

• MyVariant Identifiers: chr2:g.48982764A>G (hg19) ; chr2:g.48755625A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48755625A>G , CM000664.2:g.48755625A>G	GRCh38
NC_000002.11:g.48982764A>G , CM000664.1:g.48982764A>G	GRCh37
NC_000002.10:g.48836268A>G	NCBI36
NG_008193.1:g.5117T>C
NG_033050.1:g.230701A>G
NG_008193.2:g.5117T>C
NG_033050.2:g.230701A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.47T>C (LHCGR) MANE Select	ENSP00000294954.6:p.Leu16Pro
ENST00000294954.11:c.47T>C (LHCGR)	ENSP00000294954.6:p.Leu16Pro
ENST00000401907.5:c.47T>C (LHCGR)	ENSP00000385406.1:p.Leu16Pro
ENST00000402114.6:c.3442-20655A>G (STON1-GTF2A1L)	ENSP00000385701.1:n.3442-20655A>G
ENST00000403273.5:c.47T>C (LHCGR)	ENSP00000385847.1:p.Leu16Pro
ENST00000405626.5:c.47T>C (LHCGR)	ENSP00000386033.1:p.Leu16Pro
ENST00000602369.3:c.47T>C	ENSP00000473498.1:p.Leu16Pro
NM_000233.3:c.47T>C (LHCGR)	NP_000224.2:p.Leu16Pro
NM_001198593.1:c.3442-20655A>G (STON1-GTF2A1L)	NP_001185522.1:n.3442-20655A>G
XM_011532828.1:c.47T>C (LHCGR)	XP_011531130.1:p.Leu16Pro
XM_011532829.1:c.47T>C (LHCGR)	XP_011531131.1:p.Leu16Pro
XM_011532830.1:c.47T>C (LHCGR)	XP_011531132.1:p.Leu16Pro
NM_000233.4:c.47T>C (LHCGR) MANE Select	NP_000224.2:p.Leu16Pro
NM_001198593.2:c.3442-20655A>G (STON1-GTF2A1L)	NP_001185522.1:n.3442-20655A>G