Canonical Allele Identifier: CA2573159021

Gene: MSN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65731989A>G , CM000685.2:g.65731989A>G	GRCh38
NC_000023.10:g.64951851A>G , CM000685.1:g.64951851A>G	GRCh37
NC_000023.9:g.64868576A>G	NCBI36
NG_012516.1:g.69341A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002444.3:c.698+5A>G MANE Select	NP_002435.1:n.698+5A>G
ENST00000360270.7:c.698+5A>G MANE Select	ENSP00000353408.5:n.698+5A>G
NM_002444.2:c.698+5A>G	NP_002435.1:n.698+5A>G
ENST00000360270.6:c.698+5A>G	ENSP00000353408.5:n.698+5A>G
ENST00000697133.1:c.665+5A>G	ENSP00000513131.1:n.665+5A>G
ENST00000697134.1:c.*670+5A>G	ENSP00000513132.1:n.*670+5A>G
ENST00000697135.1:n.2280+5A>G
ENST00000697137.1:c.665+5A>G	ENSP00000513133.1:n.665+5A>G
ENST00000697138.1:c.665+5A>G	ENSP00000513134.1:n.665+5A>G
ENST00000697140.1:n.812+5A>G
XM_005262269.2:c.701+5A>G	XP_005262326.1:n.701+5A>G
XM_011530959.1:c.797+5A>G	XP_011529261.1:n.797+5A>G
XM_011530960.1:c.665+5A>G	XP_011529262.1:n.665+5A>G
XM_017029545.1:c.665+5A>G	XP_016885034.1:n.665+5A>G
XM_017029546.1:c.665+5A>G	XP_016885035.1:n.665+5A>G