Canonical Allele Identifier: CA2063585647

Gene: NAA25

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.112049014A= , CM000674.2:g.112049014A=	GRCh38
NC_000012.11:g.112486818A= , CM000674.1:g.112486818A=	GRCh37
NC_000012.10:g.110971201A=	NCBI36
NG_017071.1:g.64818T=

Transcript Alleles

HGVS	Amino-acid Change
NM_024953.4:c.1729-571T= MANE Select	NP_079229.2:n.1729-571T=
ENST00000261745.9:c.1729-571T= MANE Select	ENSP00000261745.4:n.1729-571T=
NM_024953.3:c.1729-571T=	NP_079229.2:n.1729-571T=
ENST00000261745.8:c.1729-571T=	ENSP00000261745.4:n.1729-571T=
ENST00000549711.5:c.*1435+469T=	ENSP00000448200.1:n.*1435+469T=
ENST00000551858.1:c.*1816-571T=	ENSP00000446719.1:n.*1816-571T=
ENST00000552527.5:n.1741-571T=
XM_005253938.1:c.1321-571T=	XP_005253995.1:n.1321-571T=
XM_006719606.1:c.1645-571T=	XP_006719669.1:n.1645-571T=
XM_006719606.2:c.1645-571T=	XP_006719669.1:n.1645-571T=
XM_017019977.1:c.676-571T=	XP_016875466.1:n.676-571T=
XR_002957380.1:n.1888+469T=
XR_243023.2:n.2106+469T=
XR_243023.4:n.1888+469T=
XR_944730.1:n.1982-571T=
XR_944730.3:n.1764-571T=
XR_944731.1:n.2110+469T=
XR_944731.3:n.1892+469T=