Canonical Allele Identifier: CA106701884

Gene: NAA15

Linked Data

• dbSNP Id: rs911558528
• gnomAD v3: 4-139336696-C-T
• gnomAD v4: 4-139336696-C-T
• MyVariant Identifiers: chr4:g.140257850C>T (hg19) ; chr4:g.139336696C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336696C>T , CM000666.2:g.139336696C>T	GRCh38
NC_000004.11:g.140257850C>T , CM000666.1:g.140257850C>T	GRCh37
NC_000004.10:g.140477300C>T	NCBI36
NG_053037.1:g.40230C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.140-152C>T	ENSP00000514912.1:n.140-152C>T
ENST00000700275.1:c.140-152C>T	ENSP00000514910.1:n.140-152C>T
ENST00000700276.1:c.139+2438C>T	ENSP00000514911.1:n.139+2438C>T
ENST00000700277.1:c.140-152C>T	ENSP00000514913.1:n.140-152C>T
ENST00000700278.1:n.317-152C>T
ENST00000700279.1:n.398-152C>T
ENST00000296543.10:c.140-152C>T MANE Select	ENSP00000296543.4:n.140-152C>T
ENST00000296543.9:c.140-152C>T	ENSP00000296543.4:n.140-152C>T
ENST00000398947.1:c.140-152C>T	ENSP00000381920.1:n.140-152C>T
ENST00000482087.1:n.284-152C>T
NM_057175.3:c.140-152C>T	NP_476516.1:n.140-152C>T
XM_005263236.1:c.140-152C>T	XP_005263293.1:n.140-152C>T
NM_057175.4:c.140-152C>T	NP_476516.1:n.140-152C>T
XM_005263236.3:c.140-152C>T	XP_005263293.1:n.140-152C>T
NM_057175.5:c.140-152C>T MANE Select	NP_476516.1:n.140-152C>T