Canonical Allele Identifier: CA2619403459
Gene: NAB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57094599dup , CM000674.2:g.57094599dup GRCh38
NC_000012.11:g.57488382dup , CM000674.1:g.57488382dup GRCh37
NC_000012.10:g.55774649dup NCBI36
NG_021272.1:g.21819dup
NG_021272.2:g.42545dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000300131.8:c.1469-13dup MANE Select ENSP00000300131.3:n.1469-13dup
ENST00000300131.7:c.1469-13dup ENSP00000300131.3:n.1469-13dup
ENST00000342556.6:c.1277-13dup ENSP00000341491.6:n.1277-13dup
NM_005967.3:c.1469-13dup NP_005958.1:n.1469-13dup
XM_005268894.2:c.1277-13dup XP_005268951.1:n.1277-13dup
NM_001330305.1:c.1277-13dup NP_001317234.1:n.1277-13dup
NM_005967.4:c.1469-13dup MANE Select NP_005958.1:n.1469-13dup
NM_001330305.2:c.1277-13dup NP_001317234.1:n.1277-13dup