Canonical Allele Identifier: CA2560274201
Gene: ANXA10 HGNC NCBI

Linked Data

gnomAD v4: 4-168165421-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165421C>T , CM000666.2:g.168165421C>T GRCh38
NC_000004.11:g.169086572C>T , CM000666.1:g.169086572C>T GRCh37
NC_000004.10:g.169323147C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+95C>T MANE Select ENSP00000352248.3:n.480+95C>T
ENST00000359299.7:c.480+95C>T ENSP00000352248.3:n.480+95C>T
ENST00000503003.1:n.86+95C>T
ENST00000507278.5:n.143+95C>T
ENST00000617524.1:c.477+95C>T ENSP00000483710.1:n.477+95C>T
NM_007193.4:c.480+95C>T NP_009124.2:n.480+95C>T
XM_011531571.1:c.540+95C>T XP_011529873.1:n.540+95C>T
XM_011531571.2:c.540+95C>T XP_011529873.1:n.540+95C>T
NM_007193.5:c.480+95C>T MANE Select NP_009124.2:n.480+95C>T
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