Canonical Allele Identifier: CA358258474

Gene: NAA15

Linked Data

• MyVariant Identifiers: chr4:g.140258073A>T (hg19) ; chr4:g.139336919A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336919A>T , CM000666.2:g.139336919A>T	GRCh38
NC_000004.11:g.140258073A>T , CM000666.1:g.140258073A>T	GRCh37
NC_000004.10:g.140477523A>T	NCBI36
NG_053037.1:g.40453A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.211A>T	ENSP00000514912.1:p.Arg71Ter
ENST00000700275.1:c.211A>T	ENSP00000514910.1:p.Arg71Ter
ENST00000700276.1:c.139+2661A>T	ENSP00000514911.1:n.139+2661A>T
ENST00000700277.1:c.211A>T	ENSP00000514913.1:p.Arg71Ter
ENST00000700278.1:n.388A>T
ENST00000700279.1:n.469A>T
ENST00000296543.10:c.211A>T MANE Select	ENSP00000296543.4:p.Arg71Ter
ENST00000296543.9:c.211A>T	ENSP00000296543.4:p.Arg71Ter
ENST00000398947.1:c.211A>T	ENSP00000381920.1:p.Arg71Ter
ENST00000480277.2:n.47A>T
ENST00000482087.1:n.355A>T
NM_057175.3:c.211A>T	NP_476516.1:p.Arg71Ter
XM_005263236.1:c.211A>T	XP_005263293.1:p.Arg71Ter
NM_057175.4:c.211A>T	NP_476516.1:p.Arg71Ter
XM_005263236.3:c.211A>T	XP_005263293.1:p.Arg71Ter
NM_057175.5:c.211A>T MANE Select	NP_476516.1:p.Arg71Ter