Canonical Allele Identifier: CA555034939

Gene: NAA15

Linked Data

• dbSNP Id: rs1290529515
• gnomAD v2: 4-140258152-G-A
• gnomAD v4: 4-139336998-G-A
• MyVariant Identifiers: chr4:g.140258152G>A (hg19) ; chr4:g.139336998G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336998G>A , CM000666.2:g.139336998G>A	GRCh38
NC_000004.11:g.140258152G>A , CM000666.1:g.140258152G>A	GRCh37
NC_000004.10:g.140477602G>A	NCBI36
NG_053037.1:g.40532G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.244+46G>A	ENSP00000514912.1:n.244+46G>A
ENST00000700275.1:c.244+46G>A	ENSP00000514910.1:n.244+46G>A
ENST00000700276.1:c.139+2740G>A	ENSP00000514911.1:n.139+2740G>A
ENST00000700277.1:c.240+50G>A	ENSP00000514913.1:n.240+50G>A
ENST00000700278.1:n.421+46G>A
ENST00000700279.1:n.502+46G>A
ENST00000296543.10:c.244+46G>A MANE Select	ENSP00000296543.4:n.244+46G>A
ENST00000296543.9:c.244+46G>A	ENSP00000296543.4:n.244+46G>A
ENST00000398947.1:c.244+46G>A	ENSP00000381920.1:n.244+46G>A
ENST00000480277.2:n.80+46G>A
ENST00000482087.1:n.388+46G>A
NM_057175.3:c.244+46G>A	NP_476516.1:n.244+46G>A
XM_005263236.1:c.244+46G>A	XP_005263293.1:n.244+46G>A
NM_057175.4:c.244+46G>A	NP_476516.1:n.244+46G>A
XM_005263236.3:c.244+46G>A	XP_005263293.1:n.244+46G>A
NM_057175.5:c.244+46G>A MANE Select	NP_476516.1:n.244+46G>A