Canonical Allele Identifier: CA357770363

Gene: MANBA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102690772C>G , CM000666.2:g.102690772C>G	GRCh38
NC_000004.11:g.103611929C>G , CM000666.1:g.103611929C>G	GRCh37
NC_000004.10:g.103830977C>G	NCBI36
NG_012804.1:g.75223G>C
NG_012804.2:g.75223G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005908.4:c.674-1G>C MANE Select	NP_005899.3:n.674-1G>C
ENST00000647097.2:c.674-1G>C MANE Select	ENSP00000495247.1:n.674-1G>C
NM_005908.3:c.674-1G>C	NP_005899.3:n.674-1G>C
ENST00000226578.8:c.674-1G>C	ENSP00000226578.4:n.674-1G>C
ENST00000505239.1:c.503-1G>C	ENSP00000427322.1:n.503-1G>C
ENST00000514430.5:n.799-1G>C
ENST00000642252.1:c.674-1G>C	ENSP00000495483.1:n.674-1G>C
ENST00000644159.1:c.674-1G>C	ENSP00000494462.1:n.674-1G>C
ENST00000644545.1:c.674-1G>C	ENSP00000493992.1:n.674-1G>C
ENST00000645348.1:c.674-1G>C	ENSP00000495363.1:n.674-1G>C
ENST00000645558.1:c.180-1G>C
ENST00000646311.1:c.674-1G>C	ENSP00000493465.1:n.674-1G>C
ENST00000646727.1:c.674-1G>C	ENSP00000493519.1:n.674-1G>C
ENST00000647129.1:c.356-1G>C	ENSP00000496137.1:n.356-1G>C
XM_011531965.1:c.-233-1G>C	XP_011530267.1:n.-233-1G>C
XM_017008203.1:c.311-1G>C	XP_016863692.1:n.311-1G>C
XM_017008204.2:c.26-1G>C	XP_016863693.1:n.26-1G>C
XM_024454048.1:c.599-1G>C	XP_024309816.1:n.599-1G>C
XM_024454049.1:c.311-1G>C	XP_024309817.1:n.311-1G>C