Canonical Allele Identifier: CA2568915372
Gene: ANXA5 HGNC NCBI

Linked Data

gnomAD v4: 4-121696969-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121696969T>G , CM000666.2:g.121696969T>G GRCh38
NC_000004.11:g.122618124T>G , CM000666.1:g.122618124T>G GRCh37
NC_000004.10:g.122837574T>G NCBI36
NG_032042.1:g.5024A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.-142A>C MANE Select ENSP00000296511.5:n.-142A>C
ENST00000296511.9:c.-142A>C ENSP00000296511.5:n.-142A>C
ENST00000509016.5:n.24A>C
ENST00000511552.5:n.7A>C
ENST00000513428.5:n.24A>C
ENST00000513523.1:n.27A>C
ENST00000513728.1:c.-142A>C ENSP00000427135.1:n.-142A>C
NM_001154.3:c.-142A>C NP_001145.1:n.-142A>C
XM_017008141.2:c.-142A>C XP_016863630.1:n.-142A>C
NM_001154.4:c.-142A>C MANE Select NP_001145.1:n.-142A>C
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