Canonical Allele Identifier: CA411766250

Gene: NAGA

Linked Data

• MyVariant Identifiers: chr22:g.42456998C>G (hg19) ; chr22:g.42060994C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42060994C>G , CM000684.2:g.42060994C>G	GRCh38
NC_000022.10:g.42456998C>G , CM000684.1:g.42456998C>G	GRCh37
NC_000022.9:g.40786944C>G	NCBI36
NG_009247.1:g.14849G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.1031G>C MANE Select	ENSP00000379680.3:p.Arg344Thr
ENST00000396398.7:c.1031G>C	ENSP00000379680.3:p.Arg344Thr
ENST00000402937.1:c.1031G>C	ENSP00000384603.1:p.Arg344Thr
ENST00000403363.5:c.1031G>C	ENSP00000385283.1:p.Arg344Thr
NM_000262.2:c.1031G>C	NP_000253.1:p.Arg344Thr
XM_005261615.3:c.1031G>C	XP_005261672.1:p.Arg344Thr
XM_005261616.3:c.1031G>C	XP_005261673.1:p.Arg344Thr
NM_001362848.1:c.1031G>C	NP_001349777.1:p.Arg344Thr
NM_001362850.1:c.1031G>C	NP_001349779.1:p.Arg344Thr
NM_000262.3:c.1031G>C MANE Select	NP_000253.1:p.Arg344Thr