Canonical Allele Identifier: CA357957834

Gene: MANBA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102722870C>T , CM000666.2:g.102722870C>T	GRCh38
NC_000004.11:g.103644027C>T , CM000666.1:g.103644027C>T	GRCh37
NC_000004.10:g.103863073C>T	NCBI36
NG_012804.1:g.43125G>A
NG_012804.2:g.43125G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005908.4:c.549+1G>A MANE Select	NP_005899.3:n.549+1G>A
ENST00000647097.2:c.549+1G>A MANE Select	ENSP00000495247.1:n.549+1G>A
NM_005908.3:c.549+1G>A	NP_005899.3:n.549+1G>A
ENST00000226578.8:c.549+1G>A	ENSP00000226578.4:n.549+1G>A
ENST00000505239.1:c.378+992G>A	ENSP00000427322.1:n.378+992G>A
ENST00000506478.1:n.195G>A
ENST00000514430.5:n.596+1G>A
ENST00000642252.1:c.549+1G>A	ENSP00000495483.1:n.549+1G>A
ENST00000644159.1:c.549+1G>A	ENSP00000494462.1:n.549+1G>A
ENST00000644545.1:c.549+1G>A	ENSP00000493992.1:n.549+1G>A
ENST00000645348.1:c.549+1G>A	ENSP00000495363.1:n.549+1G>A
ENST00000645558.1:c.55+1G>A
ENST00000646311.1:c.549+1G>A	ENSP00000493465.1:n.549+1G>A
ENST00000646451.1:c.474+1G>A	ENSP00000495846.1:n.474+1G>A
ENST00000646727.1:c.549+1G>A	ENSP00000493519.1:n.549+1G>A
ENST00000647129.1:c.231+1G>A	ENSP00000496137.1:n.231+1G>A
XM_017008203.1:c.186+1G>A	XP_016863692.1:n.186+1G>A
XM_017008204.2:c.25+1G>A	XP_016863693.1:n.25+1G>A
XM_024454048.1:c.474+1G>A	XP_024309816.1:n.474+1G>A
XM_024454049.1:c.186+1G>A	XP_024309817.1:n.186+1G>A