Canonical Allele Identifier: CA358258082

Gene: NAA15

Linked Data

• gnomAD v4: 4-139336846-A-G
• MyVariant Identifiers: chr4:g.140258000A>G (hg19) ; chr4:g.139336846A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336846A>G , CM000666.2:g.139336846A>G	GRCh38
NC_000004.11:g.140258000A>G , CM000666.1:g.140258000A>G	GRCh37
NC_000004.10:g.140477450A>G	NCBI36
NG_053037.1:g.40380A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.140-2A>G	ENSP00000514912.1:n.140-2A>G
ENST00000700275.1:c.140-2A>G	ENSP00000514910.1:n.140-2A>G
ENST00000700276.1:c.139+2588A>G	ENSP00000514911.1:n.139+2588A>G
ENST00000700277.1:c.140-2A>G	ENSP00000514913.1:n.140-2A>G
ENST00000700278.1:n.317-2A>G
ENST00000700279.1:n.398-2A>G
ENST00000296543.10:c.140-2A>G MANE Select	ENSP00000296543.4:n.140-2A>G
ENST00000296543.9:c.140-2A>G	ENSP00000296543.4:n.140-2A>G
ENST00000398947.1:c.140-2A>G	ENSP00000381920.1:n.140-2A>G
ENST00000482087.1:n.284-2A>G
NM_057175.3:c.140-2A>G	NP_476516.1:n.140-2A>G
XM_005263236.1:c.140-2A>G	XP_005263293.1:n.140-2A>G
NM_057175.4:c.140-2A>G	NP_476516.1:n.140-2A>G
XM_005263236.3:c.140-2A>G	XP_005263293.1:n.140-2A>G
NM_057175.5:c.140-2A>G MANE Select	NP_476516.1:n.140-2A>G