Canonical Allele Identifier: CA1489952169
Gene: ANXA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121686279_121686280delinsTA , CM000666.2:g.121686279_121686280delinsTA GRCh38
NC_000004.11:g.122607434_122607435delinsTA , CM000666.1:g.122607434_122607435delinsTA GRCh37
NC_000004.10:g.122826884_122826885delinsTA NCBI36
NG_032042.1:g.15713_15714delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000296511.10:c.94+8_94+9delinsTA MANE Select ENSP00000296511.5:n.94+8_94+9delinsTA
ENST00000296511.9:c.94+8_94+9delinsTA ENSP00000296511.5:n.94+8_94+9delinsTA
ENST00000501272.6:c.10-2803_10-2802delinsTA ENSP00000424106.1:n.10-2803_10-2802delinsTA
ENST00000506395.5:c.94+8_94+9delinsTA ENSP00000421421.1:n.94+8_94+9delinsTA
ENST00000509016.5:n.215+8_215+9delinsTA
ENST00000511552.5:n.480+8_480+9delinsTA
ENST00000513428.5:n.259+8_259+9delinsTA
ENST00000513523.1:n.262+8_262+9delinsTA
ENST00000513728.1:c.94+8_94+9delinsTA ENSP00000427135.1:n.94+8_94+9delinsTA
ENST00000515017.5:c.94+8_94+9delinsTA ENSP00000424199.1:n.94+8_94+9delinsTA
NM_001154.3:c.94+8_94+9delinsTA NP_001145.1:n.94+8_94+9delinsTA
XM_017008141.2:c.94+8_94+9delinsTA XP_016863630.1:n.94+8_94+9delinsTA
NM_001154.4:c.94+8_94+9delinsTA MANE Select NP_001145.1:n.94+8_94+9delinsTA