Canonical Allele Identifier: CA102706045

Gene: MANBA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102689573C>T , CM000666.2:g.102689573C>T	GRCh38
NC_000004.11:g.103610730C>T , CM000666.1:g.103610730C>T	GRCh37
NC_000004.10:g.103829778C>T	NCBI36
NG_012804.1:g.76422G>A
NG_012804.2:g.76422G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005908.4:c.960+1G>A MANE Select	NP_005899.3:n.960+1G>A
ENST00000647097.2:c.960+1G>A MANE Select	ENSP00000495247.1:n.960+1G>A
NM_005908.3:c.960+1G>A	NP_005899.3:n.960+1G>A
ENST00000226578.8:c.960+1G>A	ENSP00000226578.4:n.960+1G>A
ENST00000505239.1:c.789+1G>A	ENSP00000427322.1:n.789+1G>A
ENST00000514430.5:n.1085+1G>A
ENST00000642252.1:c.960+1G>A	ENSP00000495483.1:n.960+1G>A
ENST00000644159.1:c.960+1G>A	ENSP00000494462.1:n.960+1G>A
ENST00000644545.1:c.960+1G>A	ENSP00000493992.1:n.960+1G>A
ENST00000645348.1:c.960+1G>A	ENSP00000495363.1:n.960+1G>A
ENST00000645558.1:c.466+1G>A
ENST00000646311.1:c.960+1G>A	ENSP00000493465.1:n.960+1G>A
ENST00000646727.1:c.960+1G>A	ENSP00000493519.1:n.960+1G>A
ENST00000647129.1:c.642+1G>A	ENSP00000496137.1:n.642+1G>A
XM_011531965.1:c.54+1G>A	XP_011530267.1:n.54+1G>A
XM_017008203.1:c.597+1G>A	XP_016863692.1:n.597+1G>A
XM_017008204.2:c.312+1G>A	XP_016863693.1:n.312+1G>A
XM_024454048.1:c.885+1G>A	XP_024309816.1:n.885+1G>A
XM_024454049.1:c.597+1G>A	XP_024309817.1:n.597+1G>A