Canonical Allele Identifier: CA441393223

Gene: NAA15

Linked Data

• MyVariant Identifiers: chr4:g.140258105G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336951G>C , CM000666.2:g.139336951G>C	GRCh38
NC_000004.11:g.140258105G>C , CM000666.1:g.140258105G>C	GRCh37
NC_000004.10:g.140477555G>C	NCBI36
NG_053037.1:g.40485G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.243G>C	ENSP00000514912.1:p.Val81=
ENST00000700275.1:c.243G>C	ENSP00000514910.1:p.Val81=
ENST00000700276.1:c.139+2693G>C	ENSP00000514911.1:n.139+2693G>C
ENST00000700277.1:c.240+3G>C	ENSP00000514913.1:n.240+3G>C
ENST00000700278.1:n.420G>C
ENST00000700279.1:n.501G>C
ENST00000296543.10:c.243G>C MANE Select	ENSP00000296543.4:p.Val81=
ENST00000296543.9:c.243G>C	ENSP00000296543.4:p.Val81=
ENST00000398947.1:c.243G>C	ENSP00000381920.1:p.Val81=
ENST00000480277.2:n.79G>C
ENST00000482087.1:n.387G>C
NM_057175.3:c.243G>C	NP_476516.1:p.Val81=
XM_005263236.1:c.243G>C	XP_005263293.1:p.Val81=
NM_057175.4:c.243G>C	NP_476516.1:p.Val81=
XM_005263236.3:c.243G>C	XP_005263293.1:p.Val81=
NM_057175.5:c.243G>C MANE Select	NP_476516.1:p.Val81=