Canonical Allele Identifier: CA399538756

Gene: ODAD4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41965094G>T , CM000679.2:g.41965094G>T	GRCh38
NC_000017.10:g.40117112G>T , CM000679.1:g.40117112G>T	GRCh37
NC_000017.9:g.37370638G>T	NCBI36
NG_053115.1:g.39501G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_031421.5:c.1630G>T MANE Select	NP_113609.1:p.Asp544Tyr
ENST00000377540.6:c.1630G>T MANE Select	ENSP00000478589.1:p.Asp544Tyr
NM_001350319.1:c.*86G>T	NP_001337248.1:n.*86G>T
NM_001350319.2:c.*86G>T	NP_001337248.1:n.*86G>T
NM_031421.3:c.1630G>T	NP_113609.1:p.Asp544Tyr
NM_031421.4:c.1630G>T	NP_113609.1:p.Asp544Tyr
NR_110662.1:n.1298G>T
NR_110662.2:n.1327G>T
NR_110662.3:n.1304G>T
NR_146621.1:n.1249G>T
NR_146621.2:n.1226G>T
NR_146622.1:n.1682G>T
NR_146622.2:n.1659G>T
ENST00000377540.5:c.1630G>T	ENSP00000478589.1:p.Asp544Tyr
ENST00000591658.5:c.*220G>T	ENSP00000477931.1:n.*220G>T
ENST00000617460.1:c.1630G>T	ENSP00000481958.1:p.Asp544Tyr
XM_011525323.1:c.1141G>T	XP_011523625.1:p.Asp381Tyr
XM_011525324.1:c.*86G>T	XP_011523626.1:n.*86G>T