Canonical Allele Identifier: CA358037243
Gene: ANXA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686305T>A , CM000666.2:g.121686305T>A GRCh38
NC_000004.11:g.122607460T>A , CM000666.1:g.122607460T>A GRCh37
NC_000004.10:g.122826910T>A NCBI36
NG_032042.1:g.15688A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.77A>T MANE Select ENSP00000296511.5:p.Lys26Met
ENST00000296511.9:c.77A>T ENSP00000296511.5:p.Lys26Met
ENST00000501272.6:c.10-2828A>T ENSP00000424106.1:n.10-2828A>T
ENST00000506395.5:c.77A>T ENSP00000421421.1:p.Lys26Met
ENST00000509016.5:n.198A>T
ENST00000511552.5:n.463A>T
ENST00000513428.5:n.242A>T
ENST00000513523.1:n.245A>T
ENST00000513728.1:c.77A>T ENSP00000427135.1:p.Lys26Met
ENST00000515017.5:c.77A>T ENSP00000424199.1:p.Lys26Met
NM_001154.3:c.77A>T NP_001145.1:p.Lys26Met
XM_017008141.2:c.77A>T XP_016863630.1:p.Lys26Met
NM_001154.4:c.77A>T MANE Select NP_001145.1:p.Lys26Met