Canonical Allele Identifier: CA358258592

Gene: NAA15

Linked Data

• MyVariant Identifiers: chr4:g.140258098G>C (hg19) ; chr4:g.139336944G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336944G>C , CM000666.2:g.139336944G>C	GRCh38
NC_000004.11:g.140258098G>C , CM000666.1:g.140258098G>C	GRCh37
NC_000004.10:g.140477548G>C	NCBI36
NG_053037.1:g.40478G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.236G>C	ENSP00000514912.1:p.Ser79Thr
ENST00000700275.1:c.236G>C	ENSP00000514910.1:p.Ser79Thr
ENST00000700276.1:c.139+2686G>C	ENSP00000514911.1:n.139+2686G>C
ENST00000700277.1:c.236G>C	ENSP00000514913.1:p.Ser79Thr
ENST00000700278.1:n.413G>C
ENST00000700279.1:n.494G>C
ENST00000296543.10:c.236G>C MANE Select	ENSP00000296543.4:p.Ser79Thr
ENST00000296543.9:c.236G>C	ENSP00000296543.4:p.Ser79Thr
ENST00000398947.1:c.236G>C	ENSP00000381920.1:p.Ser79Thr
ENST00000480277.2:n.72G>C
ENST00000482087.1:n.380G>C
NM_057175.3:c.236G>C	NP_476516.1:p.Ser79Thr
XM_005263236.1:c.236G>C	XP_005263293.1:p.Ser79Thr
NM_057175.4:c.236G>C	NP_476516.1:p.Ser79Thr
XM_005263236.3:c.236G>C	XP_005263293.1:p.Ser79Thr
NM_057175.5:c.236G>C MANE Select	NP_476516.1:p.Ser79Thr