Canonical Allele Identifier: CA1511397946
Gene: ANXA10 HGNC NCBI

Linked Data

dbSNP Id: rs1560788051
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165592T>A , CM000666.2:g.168165592T>A GRCh38
NC_000004.11:g.169086743T>A , CM000666.1:g.169086743T>A GRCh37
NC_000004.10:g.169323318T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+266T>A MANE Select ENSP00000352248.3:n.480+266T>A
ENST00000359299.7:c.480+266T>A ENSP00000352248.3:n.480+266T>A
ENST00000503003.1:n.86+266T>A
ENST00000507278.5:n.143+266T>A
ENST00000617524.1:c.477+266T>A ENSP00000483710.1:n.477+266T>A
NM_007193.4:c.480+266T>A NP_009124.2:n.480+266T>A
XM_011531571.1:c.540+266T>A XP_011529873.1:n.540+266T>A
XM_011531571.2:c.540+266T>A XP_011529873.1:n.540+266T>A
NM_007193.5:c.480+266T>A MANE Select NP_009124.2:n.480+266T>A
Search 100 bp 5'
Search 100 bp 3'