Canonical Allele Identifier: CA3083337

Gene: NAA15

Linked Data

• dbSNP Id: rs753986206
• ExAC: 4:140258013 A / C
• gnomAD v2: 4-140258013-A-C
• gnomAD v4: 4-139336859-A-C
• MyVariant Identifiers: chr4:g.140258013A>C (hg19) ; chr4:g.139336859A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336859A>C , CM000666.2:g.139336859A>C	GRCh38
NC_000004.11:g.140258013A>C , CM000666.1:g.140258013A>C	GRCh37
NC_000004.10:g.140477463A>C	NCBI36
NG_053037.1:g.40393A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.151A>C	ENSP00000514912.1:p.Met51Leu
ENST00000700275.1:c.151A>C	ENSP00000514910.1:p.Met51Leu
ENST00000700276.1:c.139+2601A>C	ENSP00000514911.1:n.139+2601A>C
ENST00000700277.1:c.151A>C	ENSP00000514913.1:p.Met51Leu
ENST00000700278.1:n.328A>C
ENST00000700279.1:n.409A>C
ENST00000296543.10:c.151A>C MANE Select	ENSP00000296543.4:p.Met51Leu
ENST00000296543.9:c.151A>C	ENSP00000296543.4:p.Met51Leu
ENST00000398947.1:c.151A>C	ENSP00000381920.1:p.Met51Leu
ENST00000482087.1:n.295A>C
NM_057175.3:c.151A>C	NP_476516.1:p.Met51Leu
XM_005263236.1:c.151A>C	XP_005263293.1:p.Met51Leu
NM_057175.4:c.151A>C	NP_476516.1:p.Met51Leu
XM_005263236.3:c.151A>C	XP_005263293.1:p.Met51Leu
NM_057175.5:c.151A>C MANE Select	NP_476516.1:p.Met51Leu