Canonical Allele Identifier: CA346750318

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• MyVariant Identifiers: chr2:g.48915947T>A (hg19) ; chr2:g.48688808T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688808T>A , CM000664.2:g.48688808T>A	GRCh38
NC_000002.11:g.48915947T>A , CM000664.1:g.48915947T>A	GRCh37
NC_000002.10:g.48769451T>A	NCBI36
NG_008193.1:g.71934A>T
NG_033050.1:g.163884T>A
NG_008193.2:g.71934A>T
NG_033050.2:g.163884T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.989A>T (LHCGR) MANE Select	ENSP00000294954.6:p.Asp330Val
ENST00000294954.11:c.989A>T (LHCGR)	ENSP00000294954.6:p.Asp330Val
ENST00000401907.5:c.948-669A>T (LHCGR)	ENSP00000385406.1:n.948-669A>T
ENST00000402114.6:c.3441+17128T>A (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+17128T>A
ENST00000403273.5:c.948-225A>T (LHCGR)	ENSP00000385847.1:n.948-225A>T
ENST00000405626.5:c.908A>T (LHCGR)	ENSP00000386033.1:p.Asp303Val
ENST00000508440.1:c.276+17128T>A (GTF2A1L)	ENSP00000421474.1:n.276+17128T>A
ENST00000602369.3:c.*220+5416A>T	ENSP00000473498.1:n.*220+5416A>T
NM_000233.3:c.989A>T (LHCGR)	NP_000224.2:p.Asp330Val
NM_001198593.1:c.3441+17128T>A (STON1-GTF2A1L)	NP_001185522.1:n.3441+17128T>A
XM_005264309.2:c.32A>T (LHCGR)	XP_005264366.1:p.Asp11Val
XM_006712015.2:c.59A>T (LHCGR)	XP_006712078.1:p.Asp20Val
XM_011532828.1:c.914A>T (LHCGR)	XP_011531130.1:p.Asp305Val
XM_011532829.1:c.728A>T (LHCGR)	XP_011531131.1:p.Asp243Val
XM_011532830.1:c.647A>T (LHCGR)	XP_011531132.1:p.Asp216Val
XM_011532831.1:c.353A>T (LHCGR)	XP_011531133.1:p.Asp118Val
XM_011532832.1:c.59A>T (LHCGR)	XP_011531134.1:p.Asp20Val
XM_011532833.1:c.59A>T (LHCGR)	XP_011531135.1:p.Asp20Val
XM_011532834.1:c.32A>T (LHCGR)	XP_011531136.1:p.Asp11Val
XM_005264309.3:c.32A>T (LHCGR)	XP_005264366.1:p.Asp11Val
XM_006712015.3:c.59A>T (LHCGR)	XP_006712078.1:p.Asp20Val
XM_011532834.2:c.32A>T (LHCGR)	XP_011531136.1:p.Asp11Val
XM_017004089.1:c.734A>T (LHCGR)	XP_016859578.1:p.Asp245Val
XM_017004090.1:c.353A>T (LHCGR)	XP_016859579.1:p.Asp118Val
NM_000233.4:c.989A>T (LHCGR) MANE Select	NP_000224.2:p.Asp330Val
NM_001198593.2:c.3441+17128T>A (STON1-GTF2A1L)	NP_001185522.1:n.3441+17128T>A