Canonical Allele Identifier: CA357758088

Gene: MANBA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102650682C>T , CM000666.2:g.102650682C>T	GRCh38
NC_000004.11:g.103571839C>T , CM000666.1:g.103571839C>T	GRCh37
NC_000004.10:g.103790887C>T	NCBI36
NG_012804.1:g.115313G>A
NG_012804.2:g.115313G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005908.4:c.1724G>A MANE Select	NP_005899.3:p.Trp575Ter
ENST00000647097.2:c.1724G>A MANE Select	ENSP00000495247.1:p.Trp575Ter
NM_005908.3:c.1724G>A	NP_005899.3:p.Trp575Ter
ENST00000226578.8:c.1724G>A	ENSP00000226578.4:p.Trp575Ter
ENST00000505239.1:c.1553G>A	ENSP00000427322.1:p.Trp518Ter
ENST00000508141.1:n.157G>A
ENST00000514430.5:n.5959G>A
ENST00000642252.1:c.1862G>A	ENSP00000495483.1:p.Trp621Ter
ENST00000644159.1:c.1724G>A	ENSP00000494462.1:p.Trp575Ter
ENST00000644545.1:c.*364G>A	ENSP00000493992.1:n.*364G>A
ENST00000645348.1:c.*746G>A	ENSP00000495363.1:n.*746G>A
ENST00000645558.1:c.1392G>A
ENST00000646311.1:c.*844G>A	ENSP00000493465.1:n.*844G>A
ENST00000646727.1:c.*578G>A	ENSP00000493519.1:n.*578G>A
ENST00000647129.1:c.1813G>A	ENSP00000496137.1:n.1813G>A
XM_011531965.1:c.818G>A	XP_011530267.1:p.Trp273Ter
XM_011531966.1:c.479G>A	XP_011530268.1:p.Trp160Ter
XM_017008203.1:c.1361G>A	XP_016863692.1:p.Trp454Ter
XM_017008204.2:c.1076G>A	XP_016863693.1:p.Trp359Ter
XM_017008205.2:c.518G>A	XP_016863694.1:p.Trp173Ter
XM_024454048.1:c.1649G>A	XP_024309816.1:p.Trp550Ter
XM_024454049.1:c.1361G>A	XP_024309817.1:p.Trp454Ter