Canonical Allele Identifier: CA346746021
Gene: LHCGR HGNC NCBI
STON1-GTF2A1L HGNC NCBI
GTF2A1L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.48688208G>T , CM000664.2:g.48688208G>T GRCh38
NC_000002.11:g.48915347G>T , CM000664.1:g.48915347G>T GRCh37
NC_000002.10:g.48768851G>T NCBI36
NG_008193.1:g.72534C>A
NG_033050.1:g.163284G>T
NG_008193.2:g.72534C>A
NG_033050.2:g.163284G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000294954.12:c.1589C>A (LHCGR) MANE Select ENSP00000294954.6:p.Thr530Asn
ENST00000294954.11:c.1589C>A (LHCGR) ENSP00000294954.6:p.Thr530Asn
ENST00000401907.5:c.948-69C>A (LHCGR) ENSP00000385406.1:n.948-69C>A
ENST00000402114.6:c.3441+16528G>T (STON1-GTF2A1L) ENSP00000385701.1:n.3441+16528G>T
ENST00000403273.5:c.*333C>A (LHCGR) ENSP00000385847.1:n.*333C>A
ENST00000405626.5:c.1508C>A (LHCGR) ENSP00000386033.1:p.Thr503Asn
ENST00000508440.1:c.276+16528G>T (GTF2A1L) ENSP00000421474.1:n.276+16528G>T
ENST00000602369.3:c.*220+6016C>A ENSP00000473498.1:n.*220+6016C>A
NM_000233.3:c.1589C>A (LHCGR) NP_000224.2:p.Thr530Asn
NM_001198593.1:c.3441+16528G>T (STON1-GTF2A1L) NP_001185522.1:n.3441+16528G>T
XM_005264309.2:c.632C>A (LHCGR) XP_005264366.1:p.Thr211Asn
XM_006712015.2:c.659C>A (LHCGR) XP_006712078.1:p.Thr220Asn
XM_011532828.1:c.1514C>A (LHCGR) XP_011531130.1:p.Thr505Asn
XM_011532829.1:c.1328C>A (LHCGR) XP_011531131.1:p.Thr443Asn
XM_011532830.1:c.1247C>A (LHCGR) XP_011531132.1:p.Thr416Asn
XM_011532831.1:c.953C>A (LHCGR) XP_011531133.1:p.Thr318Asn
XM_011532832.1:c.659C>A (LHCGR) XP_011531134.1:p.Thr220Asn
XM_011532833.1:c.659C>A (LHCGR) XP_011531135.1:p.Thr220Asn
XM_011532834.1:c.632C>A (LHCGR) XP_011531136.1:p.Thr211Asn
XM_005264309.3:c.632C>A (LHCGR) XP_005264366.1:p.Thr211Asn
XM_006712015.3:c.659C>A (LHCGR) XP_006712078.1:p.Thr220Asn
XM_011532834.2:c.632C>A (LHCGR) XP_011531136.1:p.Thr211Asn
XM_017004089.1:c.1334C>A (LHCGR) XP_016859578.1:p.Thr445Asn
XM_017004090.1:c.953C>A (LHCGR) XP_016859579.1:p.Thr318Asn
NM_000233.4:c.1589C>A (LHCGR) MANE Select NP_000224.2:p.Thr530Asn
NM_001198593.2:c.3441+16528G>T (STON1-GTF2A1L) NP_001185522.1:n.3441+16528G>T