Canonical Allele Identifier: CA12243755

Gene: MANEA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.95607059C>A , CM000668.2:g.95607059C>A	GRCh38
NC_000006.11:g.96054935C>A , CM000668.1:g.96054935C>A	GRCh37
NC_000006.10:g.96161656C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682076.1:c.*1571C>A	ENSP00000506766.1:n.*1571C>A
ENST00000682417.1:n.2731C>A
ENST00000682663.1:c.*654C>A	ENSP00000507267.1:n.*654C>A
ENST00000683151.1:c.*1237C>A	ENSP00000507022.1:n.*1237C>A
ENST00000684164.1:n.1462C>A
ENST00000684753.1:c.*654C>A	ENSP00000506887.1:n.*654C>A
ENST00000358812.9:c.*654C>A MANE Select	ENSP00000351669.4:n.*654C>A
ENST00000358812.8:c.*654C>A	ENSP00000351669.4:n.*654C>A
NM_024641.3:c.*654C>A	NP_078917.2:n.*654C>A
XM_005267147.2:c.*654C>A	XP_005267204.1:n.*654C>A
XM_005267147.3:c.*654C>A	XP_005267204.1:n.*654C>A
NM_024641.4:c.*654C>A MANE Select	NP_078917.2:n.*654C>A