Canonical Allele Identifier: CA2672600662
Gene: ANXA10 HGNC NCBI

Linked Data

gnomAD v4: 4-168165343-TTTACATTACTTTGCACTATCTAAGCAAATAAGTATATGTCATTGCCAAAAAAAAAAAAAAAAATAGAACAGAAAACTCCAG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165345_168165425del , CM000666.2:g.168165345_168165425del GRCh38
NC_000004.11:g.169086496_169086576del , CM000666.1:g.169086496_169086576del GRCh37
NC_000004.10:g.169323071_169323151del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+19_480+99del MANE Select ENSP00000352248.3:n.480+19_480+99del
ENST00000359299.7:c.480+19_480+99del ENSP00000352248.3:n.480+19_480+99del
ENST00000503003.1:n.86+19_86+99del
ENST00000507278.5:n.143+19_143+99del
ENST00000617524.1:c.477+19_477+99del ENSP00000483710.1:n.477+19_477+99del
NM_007193.4:c.480+19_480+99del NP_009124.2:n.480+19_480+99del
XM_011531571.1:c.540+19_540+99del XP_011529873.1:n.540+19_540+99del
XM_011531571.2:c.540+19_540+99del XP_011529873.1:n.540+19_540+99del
NM_007193.5:c.480+19_480+99del MANE Select NP_009124.2:n.480+19_480+99del
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