Canonical Allele Identifier: CA2830535200
Gene: ANXA10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165493del , CM000666.2:g.168165493del GRCh38
NC_000004.11:g.169086644del , CM000666.1:g.169086644del GRCh37
NC_000004.10:g.169323219del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+167del MANE Select ENSP00000352248.3:n.480+167del
ENST00000359299.7:c.480+167del ENSP00000352248.3:n.480+167del
ENST00000503003.1:n.86+167del
ENST00000507278.5:n.143+167del
ENST00000617524.1:c.477+167del ENSP00000483710.1:n.477+167del
NM_007193.4:c.480+167del NP_009124.2:n.480+167del
XM_011531571.1:c.540+167del XP_011529873.1:n.540+167del
XM_011531571.2:c.540+167del XP_011529873.1:n.540+167del
NM_007193.5:c.480+167del MANE Select NP_009124.2:n.480+167del