Canonical Allele Identifier: CA358258613

Gene: NAA15

Linked Data

• MyVariant Identifiers: chr4:g.140258103G>T (hg19) ; chr4:g.139336949G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336949G>T , CM000666.2:g.139336949G>T	GRCh38
NC_000004.11:g.140258103G>T , CM000666.1:g.140258103G>T	GRCh37
NC_000004.10:g.140477553G>T	NCBI36
NG_053037.1:g.40483G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.241G>T	ENSP00000514912.1:p.Val81Leu
ENST00000700275.1:c.241G>T	ENSP00000514910.1:p.Val81Leu
ENST00000700276.1:c.139+2691G>T	ENSP00000514911.1:n.139+2691G>T
ENST00000700277.1:c.240+1G>T	ENSP00000514913.1:n.240+1G>T
ENST00000700278.1:n.418G>T
ENST00000700279.1:n.499G>T
ENST00000296543.10:c.241G>T MANE Select	ENSP00000296543.4:p.Val81Leu
ENST00000296543.9:c.241G>T	ENSP00000296543.4:p.Val81Leu
ENST00000398947.1:c.241G>T	ENSP00000381920.1:p.Val81Leu
ENST00000480277.2:n.77G>T
ENST00000482087.1:n.385G>T
NM_057175.3:c.241G>T	NP_476516.1:p.Val81Leu
XM_005263236.1:c.241G>T	XP_005263293.1:p.Val81Leu
NM_057175.4:c.241G>T	NP_476516.1:p.Val81Leu
XM_005263236.3:c.241G>T	XP_005263293.1:p.Val81Leu
NM_057175.5:c.241G>T MANE Select	NP_476516.1:p.Val81Leu