Canonical Allele Identifier: CA2063580375
Gene: NAA25 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.112083644G>T , CM000674.2:g.112083644G>T GRCh38
NC_000012.11:g.112521448G>T , CM000674.1:g.112521448G>T GRCh37
NC_000012.10:g.111005831G>T NCBI36
NG_017071.1:g.30188C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261745.9:c.403-2510C>A MANE Select ENSP00000261745.4:n.403-2510C>A
ENST00000261745.8:c.403-2510C>A ENSP00000261745.4:n.403-2510C>A
ENST00000547133.1:c.287-2510C>A
ENST00000549711.5:c.284-2510C>A ENSP00000448200.1:n.284-2510C>A
ENST00000551858.1:c.*490-2510C>A ENSP00000446719.1:n.*490-2510C>A
ENST00000552527.5:n.415-2510C>A
NM_024953.3:c.403-2510C>A NP_079229.2:n.403-2510C>A
XM_005253938.1:c.-6-2510C>A XP_005253995.1:n.-6-2510C>A
XM_006719606.1:c.319-2510C>A XP_006719669.1:n.319-2510C>A
XR_243023.2:n.652-2510C>A
XR_944730.1:n.652-2510C>A
XR_944731.1:n.652-2510C>A
XM_006719606.2:c.319-2510C>A XP_006719669.1:n.319-2510C>A
XM_017019977.1:c.-644-2510C>A XP_016875466.1:n.-644-2510C>A
XR_002957380.1:n.434-2510C>A
XR_243023.4:n.434-2510C>A
XR_944730.3:n.434-2510C>A
XR_944731.3:n.434-2510C>A
NM_024953.4:c.403-2510C>A MANE Select NP_079229.2:n.403-2510C>A