Canonical Allele Identifier: CA2784970

Gene: MELTF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.197027797C>T , CM000665.2:g.197027797C>T	GRCh38
NC_000003.11:g.196754668C>T , CM000665.1:g.196754668C>T	GRCh37
NC_000003.10:g.198239065C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696016.1:c.163G>A	ENSP00000512332.1:p.Val55Ile
ENST00000296350.10:c.163G>A MANE Select	ENSP00000296350.5:p.Val55Ile
ENST00000296350.9:c.163G>A	ENSP00000296350.5:p.Val55Ile
ENST00000296351.8:c.163G>A	ENSP00000296351.4:p.Val55Ile
ENST00000439320.1:c.163G>A	ENSP00000393439.1:p.Val55Ile
ENST00000473501.1:n.1498G>A
NM_005929.5:c.163G>A	NP_005920.2:p.Val55Ile
NM_033316.3:c.163G>A	NP_201573.1:p.Val55Ile
XM_006713643.2:c.163G>A	XP_006713706.2:p.Val55Ile
XM_006713644.2:c.163G>A	XP_006713707.1:p.Val55Ile
XM_011512850.1:c.163G>A	XP_011511152.1:p.Val55Ile
XM_011512851.1:c.163G>A	XP_011511153.1:p.Val55Ile
XM_006713643.3:c.163G>A	XP_006713706.2:p.Val55Ile
XM_011512850.2:c.163G>A	XP_011511152.1:p.Val55Ile
XM_011512851.2:c.163G>A	XP_011511153.1:p.Val55Ile
NM_005929.6:c.163G>A MANE Select	NP_005920.2:p.Val55Ile
NM_033316.4:c.163G>A	NP_201573.1:p.Val55Ile