Canonical Allele Identifier: CA2671937926
Gene: ANXA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121696840dup , CM000666.2:g.121696840dup GRCh38
NC_000004.11:g.122617995dup , CM000666.1:g.122617995dup GRCh37
NC_000004.10:g.122837445dup NCBI36
NG_032042.1:g.5157dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.-36+27dup MANE Select ENSP00000296511.5:n.-36+27dup
ENST00000296511.9:c.-36+27dup ENSP00000296511.5:n.-36+27dup
ENST00000501272.6:c.-36+27dup ENSP00000424106.1:n.-36+27dup
ENST00000506395.5:c.-36+27dup ENSP00000421421.1:n.-36+27dup
ENST00000509016.5:n.130+27dup
ENST00000511552.5:n.140dup
ENST00000513428.5:n.130+27dup
ENST00000513523.1:n.133+27dup
ENST00000513728.1:c.-36+27dup ENSP00000427135.1:n.-36+27dup
ENST00000515017.5:c.-36+27dup ENSP00000424199.1:n.-36+27dup
NM_001154.3:c.-36+27dup NP_001145.1:n.-36+27dup
XM_017008141.2:c.-36+27dup XP_016863630.1:n.-36+27dup
NM_001154.4:c.-36+27dup MANE Select NP_001145.1:n.-36+27dup