Canonical Allele Identifier: CA2578228343
Gene: ANXA10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165404_168165408del , CM000666.2:g.168165404_168165408del GRCh38
NC_000004.11:g.169086555_169086559del , CM000666.1:g.169086555_169086559del GRCh37
NC_000004.10:g.169323130_169323134del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+78_480+82del MANE Select ENSP00000352248.3:n.480+78_480+82del
ENST00000359299.7:c.480+78_480+82del ENSP00000352248.3:n.480+78_480+82del
ENST00000503003.1:n.86+78_86+82del
ENST00000507278.5:n.143+78_143+82del
ENST00000617524.1:c.477+78_477+82del ENSP00000483710.1:n.477+78_477+82del
NM_007193.4:c.480+78_480+82del NP_009124.2:n.480+78_480+82del
XM_011531571.1:c.540+78_540+82del XP_011529873.1:n.540+78_540+82del
XM_011531571.2:c.540+78_540+82del XP_011529873.1:n.540+78_540+82del
NM_007193.5:c.480+78_480+82del MANE Select NP_009124.2:n.480+78_480+82del