Canonical Allele Identifier: CA798719234
Gene: ANXA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.78592061A>T , CM000666.2:g.78592061A>T GRCh38
NC_000004.11:g.79513215A>T , CM000666.1:g.79513215A>T GRCh37
NC_000004.10:g.79732239A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264908.11:c.483+438A>T MANE Select ENSP00000264908.6:n.483+438A>T
ENST00000264908.10:c.483+438A>T ENSP00000264908.6:n.483+438A>T
ENST00000503570.6:c.366+438A>T ENSP00000421015.2:n.366+438A>T
ENST00000512542.5:c.16-3320A>T ENSP00000426591.1:n.16-3320A>T
ENST00000512884.5:c.366+438A>T ENSP00000423068.1:n.366+438A>T
NM_005139.2:c.483+438A>T NP_005130.1:n.483+438A>T
XM_011531906.1:c.540+438A>T XP_011530208.1:n.540+438A>T
XR_938727.1:n.642+438A>T
XR_001741215.2:n.620+438A>T
NM_005139.3:c.483+438A>T MANE Select NP_005130.1:n.483+438A>T