Canonical Allele Identifier: CA346743497

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• MyVariant Identifiers: chr2:g.48914970A>C (hg19) ; chr2:g.48687831A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48687831A>C , CM000664.2:g.48687831A>C	GRCh38
NC_000002.11:g.48914970A>C , CM000664.1:g.48914970A>C	GRCh37
NC_000002.10:g.48768474A>C	NCBI36
NG_008193.1:g.72911T>G
NG_033050.1:g.162907A>C
NG_008193.2:g.72911T>G
NG_033050.2:g.162907A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000294954.12:c.1966T>G (LHCGR) MANE Select	ENSP00000294954.6:p.Phe656Val
ENST00000294954.11:c.1966T>G (LHCGR)	ENSP00000294954.6:p.Phe656Val
ENST00000401907.5:c.*278T>G (LHCGR)	ENSP00000385406.1:n.*278T>G
ENST00000402114.6:c.3441+16151A>C (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16151A>C
ENST00000403273.5:c.*710T>G (LHCGR)	ENSP00000385847.1:n.*710T>G
ENST00000405626.5:c.1885T>G (LHCGR)	ENSP00000386033.1:p.Phe629Val
ENST00000508440.1:c.276+16151A>C (GTF2A1L)	ENSP00000421474.1:n.276+16151A>C
ENST00000602369.3:c.*220+6393T>G	ENSP00000473498.1:n.*220+6393T>G
NM_000233.3:c.1966T>G (LHCGR)	NP_000224.2:p.Phe656Val
NM_001198593.1:c.3441+16151A>C (STON1-GTF2A1L)	NP_001185522.1:n.3441+16151A>C
XM_005264309.2:c.1009T>G (LHCGR)	XP_005264366.1:p.Phe337Val
XM_006712015.2:c.1036T>G (LHCGR)	XP_006712078.1:p.Phe346Val
XM_011532828.1:c.1891T>G (LHCGR)	XP_011531130.1:p.Phe631Val
XM_011532829.1:c.1705T>G (LHCGR)	XP_011531131.1:p.Phe569Val
XM_011532830.1:c.1624T>G (LHCGR)	XP_011531132.1:p.Phe542Val
XM_011532831.1:c.1330T>G (LHCGR)	XP_011531133.1:p.Phe444Val
XM_011532832.1:c.1036T>G (LHCGR)	XP_011531134.1:p.Phe346Val
XM_011532833.1:c.1036T>G (LHCGR)	XP_011531135.1:p.Phe346Val
XM_011532834.1:c.1009T>G (LHCGR)	XP_011531136.1:p.Phe337Val
XM_005264309.3:c.1009T>G (LHCGR)	XP_005264366.1:p.Phe337Val
XM_006712015.3:c.1036T>G (LHCGR)	XP_006712078.1:p.Phe346Val
XM_011532834.2:c.1009T>G (LHCGR)	XP_011531136.1:p.Phe337Val
XM_017004089.1:c.1711T>G (LHCGR)	XP_016859578.1:p.Phe571Val
XM_017004090.1:c.1330T>G (LHCGR)	XP_016859579.1:p.Phe444Val
NM_000233.4:c.1966T>G (LHCGR) MANE Select	NP_000224.2:p.Phe656Val
NM_001198593.2:c.3441+16151A>C (STON1-GTF2A1L)	NP_001185522.1:n.3441+16151A>C