Canonical Allele Identifier: CA358258284

Gene: NAA15

Linked Data

• MyVariant Identifiers: chr4:g.140258034T>A (hg19) ; chr4:g.139336880T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336880T>A , CM000666.2:g.139336880T>A	GRCh38
NC_000004.11:g.140258034T>A , CM000666.1:g.140258034T>A	GRCh37
NC_000004.10:g.140477484T>A	NCBI36
NG_053037.1:g.40414T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.172T>A	ENSP00000514912.1:p.Cys58Ser
ENST00000700275.1:c.172T>A	ENSP00000514910.1:p.Cys58Ser
ENST00000700276.1:c.139+2622T>A	ENSP00000514911.1:n.139+2622T>A
ENST00000700277.1:c.172T>A	ENSP00000514913.1:p.Cys58Ser
ENST00000700278.1:n.349T>A
ENST00000700279.1:n.430T>A
ENST00000296543.10:c.172T>A MANE Select	ENSP00000296543.4:p.Cys58Ser
ENST00000296543.9:c.172T>A	ENSP00000296543.4:p.Cys58Ser
ENST00000398947.1:c.172T>A	ENSP00000381920.1:p.Cys58Ser
ENST00000480277.2:n.8T>A
ENST00000482087.1:n.316T>A
NM_057175.3:c.172T>A	NP_476516.1:p.Cys58Ser
XM_005263236.1:c.172T>A	XP_005263293.1:p.Cys58Ser
NM_057175.4:c.172T>A	NP_476516.1:p.Cys58Ser
XM_005263236.3:c.172T>A	XP_005263293.1:p.Cys58Ser
NM_057175.5:c.172T>A MANE Select	NP_476516.1:p.Cys58Ser