Canonical Allele Identifier: CA346746851

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• gnomAD v4: 2-48688335-G-A
• MyVariant Identifiers: chr2:g.48915474G>A (hg19) ; chr2:g.48688335G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688335G>A , CM000664.2:g.48688335G>A	GRCh38
NC_000002.11:g.48915474G>A , CM000664.1:g.48915474G>A	GRCh37
NC_000002.10:g.48768978G>A	NCBI36
NG_008193.1:g.72407C>T
NG_033050.1:g.163411G>A
NG_008193.2:g.72407C>T
NG_033050.2:g.163411G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.1462C>T (LHCGR) MANE Select	ENSP00000294954.6:p.Leu488Phe
ENST00000294954.11:c.1462C>T (LHCGR)	ENSP00000294954.6:p.Leu488Phe
ENST00000401907.5:c.948-196C>T (LHCGR)	ENSP00000385406.1:n.948-196C>T
ENST00000402114.6:c.3441+16655G>A (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16655G>A
ENST00000403273.5:c.*206C>T (LHCGR)	ENSP00000385847.1:n.*206C>T
ENST00000405626.5:c.1381C>T (LHCGR)	ENSP00000386033.1:p.Leu461Phe
ENST00000508440.1:c.276+16655G>A (GTF2A1L)	ENSP00000421474.1:n.276+16655G>A
ENST00000602369.3:c.*220+5889C>T	ENSP00000473498.1:n.*220+5889C>T
NM_000233.3:c.1462C>T (LHCGR)	NP_000224.2:p.Leu488Phe
NM_001198593.1:c.3441+16655G>A (STON1-GTF2A1L)	NP_001185522.1:n.3441+16655G>A
XM_005264309.2:c.505C>T (LHCGR)	XP_005264366.1:p.Leu169Phe
XM_006712015.2:c.532C>T (LHCGR)	XP_006712078.1:p.Leu178Phe
XM_011532828.1:c.1387C>T (LHCGR)	XP_011531130.1:p.Leu463Phe
XM_011532829.1:c.1201C>T (LHCGR)	XP_011531131.1:p.Leu401Phe
XM_011532830.1:c.1120C>T (LHCGR)	XP_011531132.1:p.Leu374Phe
XM_011532831.1:c.826C>T (LHCGR)	XP_011531133.1:p.Leu276Phe
XM_011532832.1:c.532C>T (LHCGR)	XP_011531134.1:p.Leu178Phe
XM_011532833.1:c.532C>T (LHCGR)	XP_011531135.1:p.Leu178Phe
XM_011532834.1:c.505C>T (LHCGR)	XP_011531136.1:p.Leu169Phe
XM_005264309.3:c.505C>T (LHCGR)	XP_005264366.1:p.Leu169Phe
XM_006712015.3:c.532C>T (LHCGR)	XP_006712078.1:p.Leu178Phe
XM_011532834.2:c.505C>T (LHCGR)	XP_011531136.1:p.Leu169Phe
XM_017004089.1:c.1207C>T (LHCGR)	XP_016859578.1:p.Leu403Phe
XM_017004090.1:c.826C>T (LHCGR)	XP_016859579.1:p.Leu276Phe
NM_000233.4:c.1462C>T (LHCGR) MANE Select	NP_000224.2:p.Leu488Phe
NM_001198593.2:c.3441+16655G>A (STON1-GTF2A1L)	NP_001185522.1:n.3441+16655G>A