Canonical Allele Identifier: CA830047256

Gene: MANEA

Linked Data

• dbSNP Id: rs1133503
• MyVariant Identifiers: chr6:g.96054588C>G (hg19) ; chr6:g.95606712C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.95606712C>G , CM000668.2:g.95606712C>G	GRCh38
NC_000006.11:g.96054588C>G , CM000668.1:g.96054588C>G	GRCh37
NC_000006.10:g.96161309C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000682076.1:c.*1224C>G	ENSP00000506766.1:n.*1224C>G
ENST00000682417.1:n.2384C>G
ENST00000682663.1:c.*307C>G	ENSP00000507267.1:n.*307C>G
ENST00000683151.1:c.*890C>G	ENSP00000507022.1:n.*890C>G
ENST00000684164.1:n.1115C>G
ENST00000684753.1:c.*307C>G	ENSP00000506887.1:n.*307C>G
ENST00000358812.9:c.*307C>G MANE Select	ENSP00000351669.4:n.*307C>G
ENST00000358812.8:c.*307C>G	ENSP00000351669.4:n.*307C>G
NM_024641.3:c.*307C>G	NP_078917.2:n.*307C>G
XM_005267147.2:c.*307C>G	XP_005267204.1:n.*307C>G
XM_005267147.3:c.*307C>G	XP_005267204.1:n.*307C>G
NM_024641.4:c.*307C>G MANE Select	NP_078917.2:n.*307C>G