Canonical Allele Identifier: CA788000166

Gene: NAA15

Linked Data

• dbSNP Id: rs1186506683
• MyVariant Identifiers: chr4:g.140258139T>G (hg19) ; chr4:g.139336985T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336985T>G , CM000666.2:g.139336985T>G	GRCh38
NC_000004.11:g.140258139T>G , CM000666.1:g.140258139T>G	GRCh37
NC_000004.10:g.140477589T>G	NCBI36
NG_053037.1:g.40519T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.244+33T>G	ENSP00000514912.1:n.244+33T>G
ENST00000700275.1:c.244+33T>G	ENSP00000514910.1:n.244+33T>G
ENST00000700276.1:c.139+2727T>G	ENSP00000514911.1:n.139+2727T>G
ENST00000700277.1:c.240+37T>G	ENSP00000514913.1:n.240+37T>G
ENST00000700278.1:n.421+33T>G
ENST00000700279.1:n.502+33T>G
ENST00000296543.10:c.244+33T>G MANE Select	ENSP00000296543.4:n.244+33T>G
ENST00000296543.9:c.244+33T>G	ENSP00000296543.4:n.244+33T>G
ENST00000398947.1:c.244+33T>G	ENSP00000381920.1:n.244+33T>G
ENST00000480277.2:n.80+33T>G
ENST00000482087.1:n.388+33T>G
NM_057175.3:c.244+33T>G	NP_476516.1:n.244+33T>G
XM_005263236.1:c.244+33T>G	XP_005263293.1:n.244+33T>G
NM_057175.4:c.244+33T>G	NP_476516.1:n.244+33T>G
XM_005263236.3:c.244+33T>G	XP_005263293.1:n.244+33T>G
NM_057175.5:c.244+33T>G MANE Select	NP_476516.1:n.244+33T>G