Canonical Allele Identifier: CA555999434
Gene: ANXA10 HGNC NCBI

Linked Data

dbSNP Id: rs33925175
gnomAD v2: 4-169086540-C-CAAA
gnomAD v3: 4-168165389-C-CAAA
gnomAD v4: 4-168165389-C-CAAA
MyVariant Identifiers: chr4:g.169086548_169086549insAAA (hg19) chr4:g.169086540_169086541insAAA (hg19) chr4:g.168165397_168165398insAAA (hg38) chr4:g.168165389_168165390insAAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165404_168165406dup , CM000666.2:g.168165404_168165406dup GRCh38
NC_000004.11:g.169086555_169086557dup , CM000666.1:g.169086555_169086557dup GRCh37
NC_000004.10:g.169323130_169323132dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+78_480+80dup MANE Select ENSP00000352248.3:n.480+78_480+80dup
ENST00000359299.7:c.480+78_480+80dup ENSP00000352248.3:n.480+78_480+80dup
ENST00000503003.1:n.86+78_86+80dup
ENST00000507278.5:n.143+78_143+80dup
ENST00000617524.1:c.477+78_477+80dup ENSP00000483710.1:n.477+78_477+80dup
NM_007193.4:c.480+78_480+80dup NP_009124.2:n.480+78_480+80dup
XM_011531571.1:c.540+78_540+80dup XP_011529873.1:n.540+78_540+80dup
XM_011531571.2:c.540+78_540+80dup XP_011529873.1:n.540+78_540+80dup
NM_007193.5:c.480+78_480+80dup MANE Select NP_009124.2:n.480+78_480+80dup
Search 100 bp 5'
Search 100 bp 3'