Canonical Allele Identifier: CA2764437090
Gene: ANXA10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168165401_168165402insCAC , CM000666.2:g.168165401_168165402insCAC GRCh38
NC_000004.11:g.169086552_169086553insCAC , CM000666.1:g.169086552_169086553insCAC GRCh37
NC_000004.10:g.169323127_169323128insCAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000359299.8:c.480+75_480+76insCAC MANE Select ENSP00000352248.3:n.480+75_480+76insCAC
ENST00000359299.7:c.480+75_480+76insCAC ENSP00000352248.3:n.480+75_480+76insCAC
ENST00000503003.1:n.86+75_86+76insCAC
ENST00000507278.5:n.143+75_143+76insCAC
ENST00000617524.1:c.477+75_477+76insCAC ENSP00000483710.1:n.477+75_477+76insCAC
NM_007193.4:c.480+75_480+76insCAC NP_009124.2:n.480+75_480+76insCAC
XM_011531571.1:c.540+75_540+76insCAC XP_011529873.1:n.540+75_540+76insCAC
XM_011531571.2:c.540+75_540+76insCAC XP_011529873.1:n.540+75_540+76insCAC
NM_007193.5:c.480+75_480+76insCAC MANE Select NP_009124.2:n.480+75_480+76insCAC