Canonical Allele Identifier: CA358037301
Gene: ANXA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686320G>T , CM000666.2:g.121686320G>T GRCh38
NC_000004.11:g.122607475G>T , CM000666.1:g.122607475G>T GRCh37
NC_000004.10:g.122826925G>T NCBI36
NG_032042.1:g.15673C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.62C>A MANE Select ENSP00000296511.5:p.Ala21Glu
ENST00000296511.9:c.62C>A ENSP00000296511.5:p.Ala21Glu
ENST00000501272.6:c.10-2843C>A ENSP00000424106.1:n.10-2843C>A
ENST00000506395.5:c.62C>A ENSP00000421421.1:p.Ala21Glu
ENST00000509016.5:n.183C>A
ENST00000511552.5:n.448C>A
ENST00000513428.5:n.227C>A
ENST00000513523.1:n.230C>A
ENST00000513728.1:c.62C>A ENSP00000427135.1:p.Ala21Glu
ENST00000515017.5:c.62C>A ENSP00000424199.1:p.Ala21Glu
NM_001154.3:c.62C>A NP_001145.1:p.Ala21Glu
XM_017008141.2:c.62C>A XP_016863630.1:p.Ala21Glu
NM_001154.4:c.62C>A MANE Select NP_001145.1:p.Ala21Glu