Canonical Allele Identifier: CA426018136

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• MyVariant Identifiers: chr2:g.48921386T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48694247T>G , CM000664.2:g.48694247T>G	GRCh38
NC_000002.11:g.48921386T>G , CM000664.1:g.48921386T>G	GRCh37
NC_000002.10:g.48774890T>G	NCBI36
NG_008193.1:g.66495A>C
NG_033050.1:g.169323T>G
NG_008193.2:g.66495A>C
NG_033050.2:g.169323T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.924A>C (LHCGR) MANE Select	ENSP00000294954.6:p.Val308=
ENST00000294954.11:c.924A>C (LHCGR)	ENSP00000294954.6:p.Val308=
ENST00000401907.5:c.924A>C (LHCGR)	ENSP00000385406.1:p.Val308=
ENST00000402114.6:c.3441+22567T>G (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+22567T>G
ENST00000403273.5:c.924A>C (LHCGR)	ENSP00000385847.1:p.Val308=
ENST00000405626.5:c.866+4368A>C (LHCGR)	ENSP00000386033.1:n.866+4368A>C
ENST00000508440.1:c.276+22567T>G (GTF2A1L)	ENSP00000421474.1:n.276+22567T>G
ENST00000602369.3:c.*197A>C	ENSP00000473498.1:n.*197A>C
NM_000233.3:c.924A>C (LHCGR)	NP_000224.2:p.Val308=
NM_001198593.1:c.3441+22567T>G (STON1-GTF2A1L)	NP_001185522.1:n.3441+22567T>G
XM_005264309.2:c.-17A>C (LHCGR)	XP_005264366.1:n.-17A>C
XM_011532828.1:c.849A>C (LHCGR)	XP_011531130.1:p.Val283=
XM_011532829.1:c.663A>C (LHCGR)	XP_011531131.1:p.Val221=
XM_011532830.1:c.606-5398A>C (LHCGR)	XP_011531132.1:n.606-5398A>C
XM_011532831.1:c.288A>C (LHCGR)	XP_011531133.1:p.Val96=
XM_005264309.3:c.-17A>C (LHCGR)	XP_005264366.1:n.-17A>C
XM_017004089.1:c.669A>C (LHCGR)	XP_016859578.1:p.Val223=
XM_017004090.1:c.288A>C (LHCGR)	XP_016859579.1:p.Val96=
NM_000233.4:c.924A>C (LHCGR) MANE Select	NP_000224.2:p.Val308=
NM_001198593.2:c.3441+22567T>G (STON1-GTF2A1L)	NP_001185522.1:n.3441+22567T>G