Canonical Allele Identifier: CA1511397900
Gene: ANXA10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165492T= , CM000666.2:g.168165492T= GRCh38
NC_000004.11:g.169086643T= , CM000666.1:g.169086643T= GRCh37
NC_000004.10:g.169323218T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+166T= MANE Select ENSP00000352248.3:n.480+166T=
ENST00000359299.7:c.480+166T= ENSP00000352248.3:n.480+166T=
ENST00000503003.1:n.86+166T=
ENST00000507278.5:n.143+166T=
ENST00000617524.1:c.477+166T= ENSP00000483710.1:n.477+166T=
NM_007193.4:c.480+166T= NP_009124.2:n.480+166T=
XM_011531571.1:c.540+166T= XP_011529873.1:n.540+166T=
XM_011531571.2:c.540+166T= XP_011529873.1:n.540+166T=
NM_007193.5:c.480+166T= MANE Select NP_009124.2:n.480+166T=
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