Canonical Allele Identifier: CA1498318006
Gene: NAA15 HGNC NCBI

Linked Data

dbSNP Id: rs1747221342

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.139337006A>G , CM000666.2:g.139337006A>G GRCh38
NC_000004.11:g.140258160A>G , CM000666.1:g.140258160A>G GRCh37
NC_000004.10:g.140477610A>G NCBI36
NG_053037.1:g.40540A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000468029.2:c.244+54A>G ENSP00000514912.1:n.244+54A>G
ENST00000700275.1:c.244+54A>G ENSP00000514910.1:n.244+54A>G
ENST00000700276.1:c.139+2748A>G ENSP00000514911.1:n.139+2748A>G
ENST00000700277.1:c.240+58A>G ENSP00000514913.1:n.240+58A>G
ENST00000700278.1:n.421+54A>G
ENST00000700279.1:n.502+54A>G
ENST00000296543.10:c.244+54A>G MANE Select ENSP00000296543.4:n.244+54A>G
ENST00000296543.9:c.244+54A>G ENSP00000296543.4:n.244+54A>G
ENST00000398947.1:c.244+54A>G ENSP00000381920.1:n.244+54A>G
ENST00000480277.2:n.80+54A>G
ENST00000482087.1:n.388+54A>G
NM_057175.3:c.244+54A>G NP_476516.1:n.244+54A>G
XM_005263236.1:c.244+54A>G XP_005263293.1:n.244+54A>G
NM_057175.4:c.244+54A>G NP_476516.1:n.244+54A>G
XM_005263236.3:c.244+54A>G XP_005263293.1:n.244+54A>G
NM_057175.5:c.244+54A>G MANE Select NP_476516.1:n.244+54A>G