Canonical Allele Identifier: CA346746882

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• MyVariant Identifiers: chr2:g.48915479A>T (hg19) ; chr2:g.48688340A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48688340A>T , CM000664.2:g.48688340A>T	GRCh38
NC_000002.11:g.48915479A>T , CM000664.1:g.48915479A>T	GRCh37
NC_000002.10:g.48768983A>T	NCBI36
NG_008193.1:g.72402T>A
NG_033050.1:g.163416A>T
NG_008193.2:g.72402T>A
NG_033050.2:g.163416A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000294954.12:c.1457T>A (LHCGR) MANE Select	ENSP00000294954.6:p.Ile486Asn
ENST00000294954.11:c.1457T>A (LHCGR)	ENSP00000294954.6:p.Ile486Asn
ENST00000401907.5:c.948-201T>A (LHCGR)	ENSP00000385406.1:n.948-201T>A
ENST00000402114.6:c.3441+16660A>T (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+16660A>T
ENST00000403273.5:c.*201T>A (LHCGR)	ENSP00000385847.1:n.*201T>A
ENST00000405626.5:c.1376T>A (LHCGR)	ENSP00000386033.1:p.Ile459Asn
ENST00000508440.1:c.276+16660A>T (GTF2A1L)	ENSP00000421474.1:n.276+16660A>T
ENST00000602369.3:c.*220+5884T>A	ENSP00000473498.1:n.*220+5884T>A
NM_000233.3:c.1457T>A (LHCGR)	NP_000224.2:p.Ile486Asn
NM_001198593.1:c.3441+16660A>T (STON1-GTF2A1L)	NP_001185522.1:n.3441+16660A>T
XM_005264309.2:c.500T>A (LHCGR)	XP_005264366.1:p.Ile167Asn
XM_006712015.2:c.527T>A (LHCGR)	XP_006712078.1:p.Ile176Asn
XM_011532828.1:c.1382T>A (LHCGR)	XP_011531130.1:p.Ile461Asn
XM_011532829.1:c.1196T>A (LHCGR)	XP_011531131.1:p.Ile399Asn
XM_011532830.1:c.1115T>A (LHCGR)	XP_011531132.1:p.Ile372Asn
XM_011532831.1:c.821T>A (LHCGR)	XP_011531133.1:p.Ile274Asn
XM_011532832.1:c.527T>A (LHCGR)	XP_011531134.1:p.Ile176Asn
XM_011532833.1:c.527T>A (LHCGR)	XP_011531135.1:p.Ile176Asn
XM_011532834.1:c.500T>A (LHCGR)	XP_011531136.1:p.Ile167Asn
XM_005264309.3:c.500T>A (LHCGR)	XP_005264366.1:p.Ile167Asn
XM_006712015.3:c.527T>A (LHCGR)	XP_006712078.1:p.Ile176Asn
XM_011532834.2:c.500T>A (LHCGR)	XP_011531136.1:p.Ile167Asn
XM_017004089.1:c.1202T>A (LHCGR)	XP_016859578.1:p.Ile401Asn
XM_017004090.1:c.821T>A (LHCGR)	XP_016859579.1:p.Ile274Asn
NM_000233.4:c.1457T>A (LHCGR) MANE Select	NP_000224.2:p.Ile486Asn
NM_001198593.2:c.3441+16660A>T (STON1-GTF2A1L)	NP_001185522.1:n.3441+16660A>T