Canonical Allele Identifier: CA358258118

Gene: NAA15

Linked Data

• MyVariant Identifiers: chr4:g.140258008T>G (hg19) ; chr4:g.139336854T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336854T>G , CM000666.2:g.139336854T>G	GRCh38
NC_000004.11:g.140258008T>G , CM000666.1:g.140258008T>G	GRCh37
NC_000004.10:g.140477458T>G	NCBI36
NG_053037.1:g.40388T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.146T>G	ENSP00000514912.1:p.Leu49Trp
ENST00000700275.1:c.146T>G	ENSP00000514910.1:p.Leu49Trp
ENST00000700276.1:c.139+2596T>G	ENSP00000514911.1:n.139+2596T>G
ENST00000700277.1:c.146T>G	ENSP00000514913.1:p.Leu49Trp
ENST00000700278.1:n.323T>G
ENST00000700279.1:n.404T>G
ENST00000296543.10:c.146T>G MANE Select	ENSP00000296543.4:p.Leu49Trp
ENST00000296543.9:c.146T>G	ENSP00000296543.4:p.Leu49Trp
ENST00000398947.1:c.146T>G	ENSP00000381920.1:p.Leu49Trp
ENST00000482087.1:n.290T>G
NM_057175.3:c.146T>G	NP_476516.1:p.Leu49Trp
XM_005263236.1:c.146T>G	XP_005263293.1:p.Leu49Trp
NM_057175.4:c.146T>G	NP_476516.1:p.Leu49Trp
XM_005263236.3:c.146T>G	XP_005263293.1:p.Leu49Trp
NM_057175.5:c.146T>G MANE Select	NP_476516.1:p.Leu49Trp