Canonical Allele Identifier: CA1525232615

Gene: NSUN2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.6619994_6619995delinsCA , CM000667.2:g.6619994_6619995delinsCA	GRCh38
NC_000005.9:g.6620107_6620108delinsCA , CM000667.1:g.6620107_6620108delinsCA	GRCh37
NC_000005.8:g.6673107_6673108delinsCA	NCBI36
NG_028215.1:g.18366_18367delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264670.11:c.815+111_815+112delinsTG MANE Select	ENSP00000264670.6:n.815+111_815+112delinsTG
ENST00000264670.10:c.815+111_815+112delinsTG	ENSP00000264670.6:n.815+111_815+112delinsTG
ENST00000504374.5:c.*121+111_*121+112delinsTG	ENSP00000421783.1:n.*121+111_*121+112delinsTG
ENST00000505892.5:n.1384+111_1384+112delinsTG
ENST00000506139.5:c.710+111_710+112delinsTG	ENSP00000420957.1:n.710+111_710+112delinsTG
NM_001193455.1:c.710+111_710+112delinsTG	NP_001180384.1:n.710+111_710+112delinsTG
NM_017755.5:c.815+111_815+112delinsTG	NP_060225.4:n.815+111_815+112delinsTG
NR_037947.1:n.1111+111_1111+112delinsTG
NM_017755.6:c.815+111_815+112delinsTG MANE Select	NP_060225.4:n.815+111_815+112delinsTG
NM_001193455.2:c.710+111_710+112delinsTG	NP_001180384.1:n.710+111_710+112delinsTG
NR_037947.2:n.795+111_795+112delinsTG