Canonical Allele Identifier: CA346743836

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• MyVariant Identifiers: chr2:g.48915029A>G (hg19) ; chr2:g.48687890A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48687890A>G , CM000664.2:g.48687890A>G	GRCh38
NC_000002.11:g.48915029A>G , CM000664.1:g.48915029A>G	GRCh37
NC_000002.10:g.48768533A>G	NCBI36
NG_008193.1:g.72852T>C
NG_033050.1:g.162966A>G
NG_008193.2:g.72852T>C
NG_033050.2:g.162966A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.1907T>C (LHCGR) MANE Select	ENSP00000294954.6:p.Leu636Pro
ENST00000294954.11:c.1907T>C (LHCGR)	ENSP00000294954.6:p.Leu636Pro
ENST00000401907.5:c.*219T>C (LHCGR)	ENSP00000385406.1:n.*219T>C
ENST00000402114.6:c.3441+16210A>G (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16210A>G
ENST00000403273.5:c.*651T>C (LHCGR)	ENSP00000385847.1:n.*651T>C
ENST00000405626.5:c.1826T>C (LHCGR)	ENSP00000386033.1:p.Leu609Pro
ENST00000508440.1:c.276+16210A>G (GTF2A1L)	ENSP00000421474.1:n.276+16210A>G
ENST00000602369.3:c.*220+6334T>C	ENSP00000473498.1:n.*220+6334T>C
NM_000233.3:c.1907T>C (LHCGR)	NP_000224.2:p.Leu636Pro
NM_001198593.1:c.3441+16210A>G (STON1-GTF2A1L)	NP_001185522.1:n.3441+16210A>G
XM_005264309.2:c.950T>C (LHCGR)	XP_005264366.1:p.Leu317Pro
XM_006712015.2:c.977T>C (LHCGR)	XP_006712078.1:p.Leu326Pro
XM_011532828.1:c.1832T>C (LHCGR)	XP_011531130.1:p.Leu611Pro
XM_011532829.1:c.1646T>C (LHCGR)	XP_011531131.1:p.Leu549Pro
XM_011532830.1:c.1565T>C (LHCGR)	XP_011531132.1:p.Leu522Pro
XM_011532831.1:c.1271T>C (LHCGR)	XP_011531133.1:p.Leu424Pro
XM_011532832.1:c.977T>C (LHCGR)	XP_011531134.1:p.Leu326Pro
XM_011532833.1:c.977T>C (LHCGR)	XP_011531135.1:p.Leu326Pro
XM_011532834.1:c.950T>C (LHCGR)	XP_011531136.1:p.Leu317Pro
XM_005264309.3:c.950T>C (LHCGR)	XP_005264366.1:p.Leu317Pro
XM_006712015.3:c.977T>C (LHCGR)	XP_006712078.1:p.Leu326Pro
XM_011532834.2:c.950T>C (LHCGR)	XP_011531136.1:p.Leu317Pro
XM_017004089.1:c.1652T>C (LHCGR)	XP_016859578.1:p.Leu551Pro
XM_017004090.1:c.1271T>C (LHCGR)	XP_016859579.1:p.Leu424Pro
NM_000233.4:c.1907T>C (LHCGR) MANE Select	NP_000224.2:p.Leu636Pro
NM_001198593.2:c.3441+16210A>G (STON1-GTF2A1L)	NP_001185522.1:n.3441+16210A>G