Canonical Allele Identifier: CA788000153

Gene: NAA15

Linked Data

• dbSNP Id: rs1237950849
• MyVariant Identifiers: chr4:g.140258115T>C (hg19) ; chr4:g.139336961T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336961T>C , CM000666.2:g.139336961T>C	GRCh38
NC_000004.11:g.140258115T>C , CM000666.1:g.140258115T>C	GRCh37
NC_000004.10:g.140477565T>C	NCBI36
NG_053037.1:g.40495T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.244+9T>C	ENSP00000514912.1:n.244+9T>C
ENST00000700275.1:c.244+9T>C	ENSP00000514910.1:n.244+9T>C
ENST00000700276.1:c.139+2703T>C	ENSP00000514911.1:n.139+2703T>C
ENST00000700277.1:c.240+13T>C	ENSP00000514913.1:n.240+13T>C
ENST00000700278.1:n.421+9T>C
ENST00000700279.1:n.502+9T>C
ENST00000296543.10:c.244+9T>C MANE Select	ENSP00000296543.4:n.244+9T>C
ENST00000296543.9:c.244+9T>C	ENSP00000296543.4:n.244+9T>C
ENST00000398947.1:c.244+9T>C	ENSP00000381920.1:n.244+9T>C
ENST00000480277.2:n.80+9T>C
ENST00000482087.1:n.388+9T>C
NM_057175.3:c.244+9T>C	NP_476516.1:n.244+9T>C
XM_005263236.1:c.244+9T>C	XP_005263293.1:n.244+9T>C
NM_057175.4:c.244+9T>C	NP_476516.1:n.244+9T>C
XM_005263236.3:c.244+9T>C	XP_005263293.1:n.244+9T>C
NM_057175.5:c.244+9T>C MANE Select	NP_476516.1:n.244+9T>C