Canonical Allele Identifier: CA346745355

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• gnomAD v3: 2-48688123-T-C
• gnomAD v4: 2-48688123-T-C
• MyVariant Identifiers: chr2:g.48915262T>C (hg19) ; chr2:g.48688123T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688123T>C , CM000664.2:g.48688123T>C	GRCh38
NC_000002.11:g.48915262T>C , CM000664.1:g.48915262T>C	GRCh37
NC_000002.10:g.48768766T>C	NCBI36
NG_008193.1:g.72619A>G
NG_033050.1:g.163199T>C
NG_008193.2:g.72619A>G
NG_033050.2:g.163199T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.1674A>G (LHCGR) MANE Select	ENSP00000294954.6:p.Leu558=
ENST00000294954.11:c.1674A>G (LHCGR)	ENSP00000294954.6:p.Leu558=
ENST00000401907.5:c.964A>G (LHCGR)	ENSP00000385406.1:p.Asn322Asp
ENST00000402114.6:c.3441+16443T>C (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16443T>C
ENST00000403273.5:c.*418A>G (LHCGR)	ENSP00000385847.1:n.*418A>G
ENST00000405626.5:c.1593A>G (LHCGR)	ENSP00000386033.1:p.Leu531=
ENST00000508440.1:c.276+16443T>C (GTF2A1L)	ENSP00000421474.1:n.276+16443T>C
ENST00000602369.3:c.*220+6101A>G	ENSP00000473498.1:n.*220+6101A>G
NM_000233.3:c.1674A>G (LHCGR)	NP_000224.2:p.Leu558=
NM_001198593.1:c.3441+16443T>C (STON1-GTF2A1L)	NP_001185522.1:n.3441+16443T>C
XM_005264309.2:c.717A>G (LHCGR)	XP_005264366.1:p.Leu239=
XM_006712015.2:c.744A>G (LHCGR)	XP_006712078.1:p.Leu248=
XM_011532828.1:c.1599A>G (LHCGR)	XP_011531130.1:p.Leu533=
XM_011532829.1:c.1413A>G (LHCGR)	XP_011531131.1:p.Leu471=
XM_011532830.1:c.1332A>G (LHCGR)	XP_011531132.1:p.Leu444=
XM_011532831.1:c.1038A>G (LHCGR)	XP_011531133.1:p.Leu346=
XM_011532832.1:c.744A>G (LHCGR)	XP_011531134.1:p.Leu248=
XM_011532833.1:c.744A>G (LHCGR)	XP_011531135.1:p.Leu248=
XM_011532834.1:c.717A>G (LHCGR)	XP_011531136.1:p.Leu239=
XM_005264309.3:c.717A>G (LHCGR)	XP_005264366.1:p.Leu239=
XM_006712015.3:c.744A>G (LHCGR)	XP_006712078.1:p.Leu248=
XM_011532834.2:c.717A>G (LHCGR)	XP_011531136.1:p.Leu239=
XM_017004089.1:c.1419A>G (LHCGR)	XP_016859578.1:p.Leu473=
XM_017004090.1:c.1038A>G (LHCGR)	XP_016859579.1:p.Leu346=
NM_000233.4:c.1674A>G (LHCGR) MANE Select	NP_000224.2:p.Leu558=
NM_001198593.2:c.3441+16443T>C (STON1-GTF2A1L)	NP_001185522.1:n.3441+16443T>C