Canonical Allele Identifier: CA1511397908
Gene: ANXA10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165520T= , CM000666.2:g.168165520T= GRCh38
NC_000004.11:g.169086671T= , CM000666.1:g.169086671T= GRCh37
NC_000004.10:g.169323246T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+194T= MANE Select ENSP00000352248.3:n.480+194T=
ENST00000359299.7:c.480+194T= ENSP00000352248.3:n.480+194T=
ENST00000503003.1:n.86+194T=
ENST00000507278.5:n.143+194T=
ENST00000617524.1:c.477+194T= ENSP00000483710.1:n.477+194T=
NM_007193.4:c.480+194T= NP_009124.2:n.480+194T=
XM_011531571.1:c.540+194T= XP_011529873.1:n.540+194T=
XM_011531571.2:c.540+194T= XP_011529873.1:n.540+194T=
NM_007193.5:c.480+194T= MANE Select NP_009124.2:n.480+194T=
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