Canonical Allele Identifier: CA103130110

Gene: MANBA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102723961C>T , CM000666.2:g.102723961C>T	GRCh38
NC_000004.11:g.103645118C>T , CM000666.1:g.103645118C>T	GRCh37
NC_000004.10:g.103864164C>T	NCBI36
NG_012804.1:g.42034G>A
NG_012804.2:g.42034G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005908.4:c.279G>A MANE Select	NP_005899.3:p.Trp93Ter
ENST00000647097.2:c.279G>A MANE Select	ENSP00000495247.1:p.Trp93Ter
NM_005908.3:c.279G>A	NP_005899.3:p.Trp93Ter
ENST00000226578.8:c.279G>A	ENSP00000226578.4:p.Trp93Ter
ENST00000505239.1:c.279G>A	ENSP00000427322.1:p.Trp93Ter
ENST00000511813.1:c.*245G>A	ENSP00000422001.1:n.*245G>A
ENST00000514430.5:n.326G>A
ENST00000642252.1:c.279G>A	ENSP00000495483.1:p.Trp93Ter
ENST00000644159.1:c.279G>A	ENSP00000494462.1:p.Trp93Ter
ENST00000644545.1:c.279G>A	ENSP00000493992.1:p.Trp93Ter
ENST00000644965.1:c.*184G>A	ENSP00000495818.1:n.*184G>A
ENST00000645348.1:c.279G>A	ENSP00000495363.1:p.Trp93Ter
ENST00000646311.1:c.279G>A	ENSP00000493465.1:p.Trp93Ter
ENST00000646451.1:c.204G>A	ENSP00000495846.1:p.Trp68Ter
ENST00000646727.1:c.279G>A	ENSP00000493519.1:p.Trp93Ter
XM_017008203.1:c.-85G>A	XP_016863692.1:n.-85G>A
XM_017008204.2:c.-246G>A	XP_016863693.1:n.-246G>A
XM_024454048.1:c.204G>A	XP_024309816.1:p.Trp68Ter
XM_024454049.1:c.-85G>A	XP_024309817.1:n.-85G>A