Canonical Allele Identifier: CA357768849

Gene: MANBA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102689621C>T , CM000666.2:g.102689621C>T	GRCh38
NC_000004.11:g.103610778C>T , CM000666.1:g.103610778C>T	GRCh37
NC_000004.10:g.103829826C>T	NCBI36
NG_012804.1:g.76374G>A
NG_012804.2:g.76374G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005908.4:c.913G>A MANE Select	NP_005899.3:p.Val305Ile
ENST00000647097.2:c.913G>A MANE Select	ENSP00000495247.1:p.Val305Ile
NM_005908.3:c.913G>A	NP_005899.3:p.Val305Ile
ENST00000226578.8:c.913G>A	ENSP00000226578.4:p.Val305Ile
ENST00000505239.1:c.742G>A	ENSP00000427322.1:p.Val248Ile
ENST00000514430.5:n.1038G>A
ENST00000642252.1:c.913G>A	ENSP00000495483.1:p.Val305Ile
ENST00000644159.1:c.913G>A	ENSP00000494462.1:p.Val305Ile
ENST00000644545.1:c.913G>A	ENSP00000493992.1:p.Val305Ile
ENST00000645348.1:c.913G>A	ENSP00000495363.1:p.Val305Ile
ENST00000645558.1:c.419G>A
ENST00000646311.1:c.913G>A	ENSP00000493465.1:p.Val305Ile
ENST00000646727.1:c.913G>A	ENSP00000493519.1:p.Val305Ile
ENST00000647129.1:c.595G>A	ENSP00000496137.1:p.Val199Ile
XM_011531965.1:c.7G>A	XP_011530267.1:p.Val3Ile
XM_017008203.1:c.550G>A	XP_016863692.1:p.Val184Ile
XM_017008204.2:c.265G>A	XP_016863693.1:p.Val89Ile
XM_024454048.1:c.838G>A	XP_024309816.1:p.Val280Ile
XM_024454049.1:c.550G>A	XP_024309817.1:p.Val184Ile