Canonical Allele Identifier: CA1511397882
Gene: ANXA10 HGNC NCBI

Linked Data

dbSNP Id: rs1731860418
gnomAD v4: 4-168165440-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165440T>A , CM000666.2:g.168165440T>A GRCh38
NC_000004.11:g.169086591T>A , CM000666.1:g.169086591T>A GRCh37
NC_000004.10:g.169323166T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+114T>A MANE Select ENSP00000352248.3:n.480+114T>A
ENST00000359299.7:c.480+114T>A ENSP00000352248.3:n.480+114T>A
ENST00000503003.1:n.86+114T>A
ENST00000507278.5:n.143+114T>A
ENST00000617524.1:c.477+114T>A ENSP00000483710.1:n.477+114T>A
NM_007193.4:c.480+114T>A NP_009124.2:n.480+114T>A
XM_011531571.1:c.540+114T>A XP_011529873.1:n.540+114T>A
XM_011531571.2:c.540+114T>A XP_011529873.1:n.540+114T>A
NM_007193.5:c.480+114T>A MANE Select NP_009124.2:n.480+114T>A
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