Canonical Allele Identifier: CA102706588

Gene: MANBA

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642252.1:c.757G>C	ENSP00000495483.1:p.Val253Leu
ENST00000644159.1:c.757G>C	ENSP00000494462.1:p.Val253Leu
ENST00000644545.1:c.757G>C	ENSP00000493992.1:p.Val253Leu
ENST00000645348.1:c.757G>C	ENSP00000495363.1:p.Val253Leu
ENST00000645558.1:c.263G>C
ENST00000646311.1:c.757G>C	ENSP00000493465.1:p.Val253Leu
ENST00000646727.1:c.757G>C	ENSP00000493519.1:p.Val253Leu
ENST00000647097.2:c.757G>C MANE Select	ENSP00000495247.1:p.Val253Leu
ENST00000647129.1:c.439G>C	ENSP00000496137.1:p.Val147Leu
ENST00000226578.8:c.757G>C	ENSP00000226578.4:p.Val253Leu
ENST00000505239.1:c.586G>C	ENSP00000427322.1:p.Val196Leu
ENST00000514430.5:n.882G>C
NM_005908.3:c.757G>C	NP_005899.3:p.Val253Leu
XM_011531965.1:c.-150G>C	XP_011530267.1:n.-150G>C
XM_017008203.1:c.394G>C	XP_016863692.1:p.Val132Leu
XM_017008204.2:c.109G>C	XP_016863693.1:p.Val37Leu
XM_024454048.1:c.682G>C	XP_024309816.1:p.Val228Leu
XM_024454049.1:c.394G>C	XP_024309817.1:p.Val132Leu
NM_005908.4:c.757G>C MANE Select	NP_005899.3:p.Val253Leu