Canonical Allele Identifier: CA514677714

Gene: NAGA

Linked Data

• MyVariant Identifiers: chr22:g.42462738G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42066734G>C , CM000684.2:g.42066734G>C	GRCh38
NC_000022.10:g.42462738G>C , CM000684.1:g.42462738G>C	GRCh37
NC_000022.9:g.40792684G>C	NCBI36
NG_009247.1:g.9109C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396398.8:c.573C>G MANE Select	ENSP00000379680.3:p.Ala191=
ENST00000396398.7:c.573C>G	ENSP00000379680.3:p.Ala191=
ENST00000402937.1:c.573C>G	ENSP00000384603.1:p.Ala191=
ENST00000403363.5:c.573C>G	ENSP00000385283.1:p.Ala191=
NM_000262.2:c.573C>G	NP_000253.1:p.Ala191=
XM_005261615.3:c.573C>G	XP_005261672.1:p.Ala191=
XM_005261616.3:c.573C>G	XP_005261673.1:p.Ala191=
NM_001362848.1:c.573C>G	NP_001349777.1:p.Ala191=
NM_001362850.1:c.573C>G	NP_001349779.1:p.Ala191=
NM_000262.3:c.573C>G MANE Select	NP_000253.1:p.Ala191=