Canonical Allele Identifier: CA346751593

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• MyVariant Identifiers: chr2:g.48921391T>A (hg19) ; chr2:g.48694252T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48694252T>A , CM000664.2:g.48694252T>A	GRCh38
NC_000002.11:g.48921391T>A , CM000664.1:g.48921391T>A	GRCh37
NC_000002.10:g.48774895T>A	NCBI36
NG_008193.1:g.66490A>T
NG_033050.1:g.169328T>A
NG_008193.2:g.66490A>T
NG_033050.2:g.169328T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000294954.12:c.919A>T (LHCGR) MANE Select	ENSP00000294954.6:p.Thr307Ser
ENST00000294954.11:c.919A>T (LHCGR)	ENSP00000294954.6:p.Thr307Ser
ENST00000401907.5:c.919A>T (LHCGR)	ENSP00000385406.1:p.Thr307Ser
ENST00000402114.6:c.3441+22572T>A (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+22572T>A
ENST00000403273.5:c.919A>T (LHCGR)	ENSP00000385847.1:p.Thr307Ser
ENST00000405626.5:c.866+4363A>T (LHCGR)	ENSP00000386033.1:n.866+4363A>T
ENST00000508440.1:c.276+22572T>A (GTF2A1L)	ENSP00000421474.1:n.276+22572T>A
ENST00000602369.3:c.*192A>T	ENSP00000473498.1:n.*192A>T
NM_000233.3:c.919A>T (LHCGR)	NP_000224.2:p.Thr307Ser
NM_001198593.1:c.3441+22572T>A (STON1-GTF2A1L)	NP_001185522.1:n.3441+22572T>A
XM_005264309.2:c.-22A>T (LHCGR)	XP_005264366.1:n.-22A>T
XM_011532828.1:c.844A>T (LHCGR)	XP_011531130.1:p.Thr282Ser
XM_011532829.1:c.658A>T (LHCGR)	XP_011531131.1:p.Thr220Ser
XM_011532830.1:c.606-5403A>T (LHCGR)	XP_011531132.1:n.606-5403A>T
XM_011532831.1:c.283A>T (LHCGR)	XP_011531133.1:p.Thr95Ser
XM_005264309.3:c.-22A>T (LHCGR)	XP_005264366.1:n.-22A>T
XM_017004089.1:c.664A>T (LHCGR)	XP_016859578.1:p.Thr222Ser
XM_017004090.1:c.283A>T (LHCGR)	XP_016859579.1:p.Thr95Ser
NM_000233.4:c.919A>T (LHCGR) MANE Select	NP_000224.2:p.Thr307Ser
NM_001198593.2:c.3441+22572T>A (STON1-GTF2A1L)	NP_001185522.1:n.3441+22572T>A