Canonical Allele Identifier: CA2658992240

Gene: LHCGR STON1-GTF2A1L GTF2A1L

Linked Data

• gnomAD v4: 2-48694199-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.48694199A>G , CM000664.2:g.48694199A>G	GRCh38
NC_000002.11:g.48921338A>G , CM000664.1:g.48921338A>G	GRCh37
NC_000002.10:g.48774842A>G	NCBI36
NG_008193.1:g.66543T>C
NG_033050.1:g.169275A>G
NG_008193.2:g.66543T>C
NG_033050.2:g.169275A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294954.12:c.947+25T>C (LHCGR) MANE Select	ENSP00000294954.6:n.947+25T>C
ENST00000294954.11:c.947+25T>C (LHCGR)	ENSP00000294954.6:n.947+25T>C
ENST00000401907.5:c.947+25T>C (LHCGR)	ENSP00000385406.1:n.947+25T>C
ENST00000402114.6:c.3441+22519A>G (STON1-GTF2A1L)	ENSP00000385701.1:n.3441+22519A>G
ENST00000403273.5:c.947+25T>C (LHCGR)	ENSP00000385847.1:n.947+25T>C
ENST00000405626.5:c.866+4416T>C (LHCGR)	ENSP00000386033.1:n.866+4416T>C
ENST00000508440.1:c.276+22519A>G (GTF2A1L)	ENSP00000421474.1:n.276+22519A>G
ENST00000602369.3:c.*220+25T>C	ENSP00000473498.1:n.*220+25T>C
NM_000233.3:c.947+25T>C (LHCGR)	NP_000224.2:n.947+25T>C
NM_001198593.1:c.3441+22519A>G (STON1-GTF2A1L)	NP_001185522.1:n.3441+22519A>G
XM_005264309.2:c.-11+42T>C (LHCGR)	XP_005264366.1:n.-11+42T>C
XM_006712015.2:c.-935T>C (LHCGR)	XP_006712078.1:n.-935T>C
XM_011532828.1:c.872+25T>C (LHCGR)	XP_011531130.1:n.872+25T>C
XM_011532829.1:c.686+25T>C (LHCGR)	XP_011531131.1:n.686+25T>C
XM_011532830.1:c.606-5350T>C (LHCGR)	XP_011531132.1:n.606-5350T>C
XM_011532831.1:c.311+25T>C (LHCGR)	XP_011531133.1:n.311+25T>C
XM_011532832.1:c.-502T>C (LHCGR)	XP_011531134.1:n.-502T>C
XM_011532833.1:c.-498T>C (LHCGR)	XP_011531135.1:n.-498T>C
XM_011532834.1:c.-304T>C (LHCGR)	XP_011531136.1:n.-304T>C
XM_005264309.3:c.-11+42T>C (LHCGR)	XP_005264366.1:n.-11+42T>C
XM_006712015.3:c.-935T>C (LHCGR)	XP_006712078.1:n.-935T>C
XM_011532834.2:c.-304T>C (LHCGR)	XP_011531136.1:n.-304T>C
XM_017004089.1:c.692+25T>C (LHCGR)	XP_016859578.1:n.692+25T>C
XM_017004090.1:c.311+25T>C (LHCGR)	XP_016859579.1:n.311+25T>C
NM_000233.4:c.947+25T>C (LHCGR) MANE Select	NP_000224.2:n.947+25T>C
NM_001198593.2:c.3441+22519A>G (STON1-GTF2A1L)	NP_001185522.1:n.3441+22519A>G