Canonical Allele Identifier: CA1648385264

Gene: MANEA

Genomic Alleles

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

Transcript Alleles

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