Canonical Allele Identifier: CA359125047

Gene: NSUN2

Linked Data

• MyVariant Identifiers: chr5:g.6620233A>T (hg19) ; chr5:g.6620120A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6620120A>T , CM000667.2:g.6620120A>T	GRCh38
NC_000005.9:g.6620233A>T , CM000667.1:g.6620233A>T	GRCh37
NC_000005.8:g.6673233A>T	NCBI36
NG_028215.1:g.18241T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.801T>A MANE Select	ENSP00000264670.6:p.Cys267Ter
ENST00000264670.10:c.801T>A	ENSP00000264670.6:p.Cys267Ter
ENST00000504374.5:c.*107T>A	ENSP00000421783.1:n.*107T>A
ENST00000505264.1:n.468T>A
ENST00000505892.5:n.1370T>A
ENST00000506139.5:c.696T>A	ENSP00000420957.1:p.Cys232Ter
NM_001193455.1:c.696T>A	NP_001180384.1:p.Cys232Ter
NM_017755.5:c.801T>A	NP_060225.4:p.Cys267Ter
NR_037947.1:n.1097T>A
NM_017755.6:c.801T>A MANE Select	NP_060225.4:p.Cys267Ter
NM_001193455.2:c.696T>A	NP_001180384.1:p.Cys232Ter
NR_037947.2:n.781T>A