Canonical Allele Identifier: CA358258482

Gene: NAA15

Linked Data

• MyVariant Identifiers: chr4:g.140258075A>C (hg19) ; chr4:g.139336921A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336921A>C , CM000666.2:g.139336921A>C	GRCh38
NC_000004.11:g.140258075A>C , CM000666.1:g.140258075A>C	GRCh37
NC_000004.10:g.140477525A>C	NCBI36
NG_053037.1:g.40455A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.213A>C	ENSP00000514912.1:p.Arg71Ser
ENST00000700275.1:c.213A>C	ENSP00000514910.1:p.Arg71Ser
ENST00000700276.1:c.139+2663A>C	ENSP00000514911.1:n.139+2663A>C
ENST00000700277.1:c.213A>C	ENSP00000514913.1:p.Arg71Ser
ENST00000700278.1:n.390A>C
ENST00000700279.1:n.471A>C
ENST00000296543.10:c.213A>C MANE Select	ENSP00000296543.4:p.Arg71Ser
ENST00000296543.9:c.213A>C	ENSP00000296543.4:p.Arg71Ser
ENST00000398947.1:c.213A>C	ENSP00000381920.1:p.Arg71Ser
ENST00000480277.2:n.49A>C
ENST00000482087.1:n.357A>C
NM_057175.3:c.213A>C	NP_476516.1:p.Arg71Ser
XM_005263236.1:c.213A>C	XP_005263293.1:p.Arg71Ser
NM_057175.4:c.213A>C	NP_476516.1:p.Arg71Ser
XM_005263236.3:c.213A>C	XP_005263293.1:p.Arg71Ser
NM_057175.5:c.213A>C MANE Select	NP_476516.1:p.Arg71Ser