Canonical Allele Identifier: CA4016335

Gene: MAP7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.136550359G>A , CM000668.2:g.136550359G>A	GRCh38
NC_000006.11:g.136871497G>A , CM000668.1:g.136871497G>A	GRCh37
NC_000006.10:g.136913190G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003980.6:c.50C>T MANE Select	NP_003971.1:p.Ala17Val
ENST00000354570.8:c.50C>T MANE Select	ENSP00000346581.2:p.Ala17Val
NM_001198616.1:c.50C>T	NP_001185545.1:p.Ala17Val
NM_001198616.3:c.50C>T	NP_001185545.1:p.Ala17Val
NM_001198617.1:c.50C>T	NP_001185546.1:p.Ala17Val
NM_001198617.3:c.50C>T	NP_001185546.1:p.Ala17Val
NM_001388334.1:c.50C>T	NP_001375263.1:p.Ala17Val
NM_001388335.1:c.50C>T	NP_001375264.1:p.Ala17Val
NM_001388339.1:c.50C>T	NP_001375268.1:p.Ala17Val
NM_001388342.1:c.50C>T	NP_001375271.1:p.Ala17Val
NM_001388347.1:c.50C>T	NP_001375276.1:p.Ala17Val
NM_001388352.1:c.50C>T	NP_001375281.1:p.Ala17Val
NM_003980.4:c.50C>T	NP_003971.1:p.Ala17Val
ENST00000354570.7:c.50C>T	ENSP00000346581.2:p.Ala17Val
ENST00000616617.4:c.50C>T	ENSP00000483511.1:p.Ala17Val
ENST00000618822.4:c.50C>T	ENSP00000482356.1:p.Ala17Val
XM_006715601.2:c.50C>T	XP_006715664.1:p.Ala17Val
XM_006715601.4:c.50C>T	XP_006715664.1:p.Ala17Val
XM_011536245.1:c.50C>T	XP_011534547.1:p.Ala17Val
XM_011536245.2:c.50C>T	XP_011534547.1:p.Ala17Val