Canonical Allele Identifier: CA787999869

Gene: NAA15

Linked Data

• dbSNP Id: rs1453575816
• gnomAD v3: 4-139336678-A-T
• gnomAD v4: 4-139336678-A-T
• MyVariant Identifiers: chr4:g.140257832A>T (hg19) ; chr4:g.139336678A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336678A>T , CM000666.2:g.139336678A>T	GRCh38
NC_000004.11:g.140257832A>T , CM000666.1:g.140257832A>T	GRCh37
NC_000004.10:g.140477282A>T	NCBI36
NG_053037.1:g.40212A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.140-170A>T	ENSP00000514912.1:n.140-170A>T
ENST00000700275.1:c.140-170A>T	ENSP00000514910.1:n.140-170A>T
ENST00000700276.1:c.139+2420A>T	ENSP00000514911.1:n.139+2420A>T
ENST00000700277.1:c.140-170A>T	ENSP00000514913.1:n.140-170A>T
ENST00000700278.1:n.317-170A>T
ENST00000700279.1:n.398-170A>T
ENST00000296543.10:c.140-170A>T MANE Select	ENSP00000296543.4:n.140-170A>T
ENST00000296543.9:c.140-170A>T	ENSP00000296543.4:n.140-170A>T
ENST00000398947.1:c.140-170A>T	ENSP00000381920.1:n.140-170A>T
ENST00000482087.1:n.284-170A>T
NM_057175.3:c.140-170A>T	NP_476516.1:n.140-170A>T
XM_005263236.1:c.140-170A>T	XP_005263293.1:n.140-170A>T
NM_057175.4:c.140-170A>T	NP_476516.1:n.140-170A>T
XM_005263236.3:c.140-170A>T	XP_005263293.1:n.140-170A>T
NM_057175.5:c.140-170A>T MANE Select	NP_476516.1:n.140-170A>T