Canonical Allele Identifier: CA1481466875

Gene: MANBA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102690688C= , CM000666.2:g.102690688C=	GRCh38
NC_000004.11:g.103611845C= , CM000666.1:g.103611845C=	GRCh37
NC_000004.10:g.103830893C=	NCBI36
NG_012804.1:g.75307G=
NG_012804.2:g.75307G=

Transcript Alleles

HGVS	Amino-acid Change
NM_005908.4:c.757G= MANE Select	NP_005899.3:p.Val253=
ENST00000647097.2:c.757G= MANE Select	ENSP00000495247.1:p.Val253=
NM_005908.3:c.757G=	NP_005899.3:p.Val253=
ENST00000226578.8:c.757G=	ENSP00000226578.4:p.Val253=
ENST00000505239.1:c.586G=	ENSP00000427322.1:p.Val196=
ENST00000514430.5:n.882G=
ENST00000642252.1:c.757G=	ENSP00000495483.1:p.Val253=
ENST00000644159.1:c.757G=	ENSP00000494462.1:p.Val253=
ENST00000644545.1:c.757G=	ENSP00000493992.1:p.Val253=
ENST00000645348.1:c.757G=	ENSP00000495363.1:p.Val253=
ENST00000645558.1:c.263G=
ENST00000646311.1:c.757G=	ENSP00000493465.1:p.Val253=
ENST00000646727.1:c.757G=	ENSP00000493519.1:p.Val253=
ENST00000647129.1:c.439G=	ENSP00000496137.1:p.Val147=
XM_011531965.1:c.-150G=	XP_011530267.1:n.-150G=
XM_017008203.1:c.394G=	XP_016863692.1:p.Val132=
XM_017008204.2:c.109G=	XP_016863693.1:p.Val37=
XM_024454048.1:c.682G=	XP_024309816.1:p.Val228=
XM_024454049.1:c.394G=	XP_024309817.1:p.Val132=