Canonical Allele Identifier: CA2672126038

Gene: NAA15

Linked Data

• gnomAD v4: 4-139336991-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336991G>T , CM000666.2:g.139336991G>T	GRCh38
NC_000004.11:g.140258145G>T , CM000666.1:g.140258145G>T	GRCh37
NC_000004.10:g.140477595G>T	NCBI36
NG_053037.1:g.40525G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.244+39G>T	ENSP00000514912.1:n.244+39G>T
ENST00000700275.1:c.244+39G>T	ENSP00000514910.1:n.244+39G>T
ENST00000700276.1:c.139+2733G>T	ENSP00000514911.1:n.139+2733G>T
ENST00000700277.1:c.240+43G>T	ENSP00000514913.1:n.240+43G>T
ENST00000700278.1:n.421+39G>T
ENST00000700279.1:n.502+39G>T
ENST00000296543.10:c.244+39G>T MANE Select	ENSP00000296543.4:n.244+39G>T
ENST00000296543.9:c.244+39G>T	ENSP00000296543.4:n.244+39G>T
ENST00000398947.1:c.244+39G>T	ENSP00000381920.1:n.244+39G>T
ENST00000480277.2:n.80+39G>T
ENST00000482087.1:n.388+39G>T
NM_057175.3:c.244+39G>T	NP_476516.1:n.244+39G>T
XM_005263236.1:c.244+39G>T	XP_005263293.1:n.244+39G>T
NM_057175.4:c.244+39G>T	NP_476516.1:n.244+39G>T
XM_005263236.3:c.244+39G>T	XP_005263293.1:n.244+39G>T
NM_057175.5:c.244+39G>T MANE Select	NP_476516.1:n.244+39G>T