Canonical Allele Identifier: CA346743518

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• MyVariant Identifiers: chr2:g.48914972T>G (hg19) ; chr2:g.48687833T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48687833T>G , CM000664.2:g.48687833T>G	GRCh38
NC_000002.11:g.48914972T>G , CM000664.1:g.48914972T>G	GRCh37
NC_000002.10:g.48768476T>G	NCBI36
NG_008193.1:g.72909A>C
NG_033050.1:g.162909T>G
NG_008193.2:g.72909A>C
NG_033050.2:g.162909T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000294954.12:c.1964A>C (LHCGR) MANE Select	ENSP00000294954.6:p.Asp655Ala
ENST00000294954.11:c.1964A>C (LHCGR)	ENSP00000294954.6:p.Asp655Ala
ENST00000401907.5:c.*276A>C (LHCGR)	ENSP00000385406.1:n.*276A>C
ENST00000402114.6:c.3441+16153T>G (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16153T>G
ENST00000403273.5:c.*708A>C (LHCGR)	ENSP00000385847.1:n.*708A>C
ENST00000405626.5:c.1883A>C (LHCGR)	ENSP00000386033.1:p.Asp628Ala
ENST00000508440.1:c.276+16153T>G (GTF2A1L)	ENSP00000421474.1:n.276+16153T>G
ENST00000602369.3:c.*220+6391A>C	ENSP00000473498.1:n.*220+6391A>C
NM_000233.3:c.1964A>C (LHCGR)	NP_000224.2:p.Asp655Ala
NM_001198593.1:c.3441+16153T>G (STON1-GTF2A1L)	NP_001185522.1:n.3441+16153T>G
XM_005264309.2:c.1007A>C (LHCGR)	XP_005264366.1:p.Asp336Ala
XM_006712015.2:c.1034A>C (LHCGR)	XP_006712078.1:p.Asp345Ala
XM_011532828.1:c.1889A>C (LHCGR)	XP_011531130.1:p.Asp630Ala
XM_011532829.1:c.1703A>C (LHCGR)	XP_011531131.1:p.Asp568Ala
XM_011532830.1:c.1622A>C (LHCGR)	XP_011531132.1:p.Asp541Ala
XM_011532831.1:c.1328A>C (LHCGR)	XP_011531133.1:p.Asp443Ala
XM_011532832.1:c.1034A>C (LHCGR)	XP_011531134.1:p.Asp345Ala
XM_011532833.1:c.1034A>C (LHCGR)	XP_011531135.1:p.Asp345Ala
XM_011532834.1:c.1007A>C (LHCGR)	XP_011531136.1:p.Asp336Ala
XM_005264309.3:c.1007A>C (LHCGR)	XP_005264366.1:p.Asp336Ala
XM_006712015.3:c.1034A>C (LHCGR)	XP_006712078.1:p.Asp345Ala
XM_011532834.2:c.1007A>C (LHCGR)	XP_011531136.1:p.Asp336Ala
XM_017004089.1:c.1709A>C (LHCGR)	XP_016859578.1:p.Asp570Ala
XM_017004090.1:c.1328A>C (LHCGR)	XP_016859579.1:p.Asp443Ala
NM_000233.4:c.1964A>C (LHCGR) MANE Select	NP_000224.2:p.Asp655Ala
NM_001198593.2:c.3441+16153T>G (STON1-GTF2A1L)	NP_001185522.1:n.3441+16153T>G