Canonical Allele Identifier: CA1489951963
Gene: ANXA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.121685882_121685904delinsGTTCAGTTCTAGAGACTGAATAT , CM000666.2:g.121685882_121685904delinsGTTCAGTTCTAGAGACTGAATAT GRCh38
NC_000004.11:g.122607037_122607059delinsGTTCAGTTCTAGAGACTGAATAT , CM000666.1:g.122607037_122607059delinsGTTCAGTTCTAGAGACTGAATAT GRCh37
NC_000004.10:g.122826487_122826509delinsGTTCAGTTCTAGAGACTGAATAT NCBI36
NG_032042.1:g.16089_16111delinsATATTCAGTCTCTAGAACTGAAC

Transcript Alleles

HGVS Amino-acid change
ENST00000296511.10:c.94+384_94+406delinsATATTCAGTCTCTAGAACTGAAC MANE Select ENSP00000296511.5:n.94+384_94+406delinsAT...
ENST00000296511.9:c.94+384_94+406delinsATATTCAGTCTCTAGAACTGAAC ENSP00000296511.5:n.94+384_94+406delinsAT...
ENST00000501272.6:c.10-2427_10-2405delinsATATTCAGTCTCTAGAACTGAAC ENSP00000424106.1:n.10-2427_10-2405delins...
ENST00000506395.5:c.94+384_94+406delinsATATTCAGTCTCTAGAACTGAAC ENSP00000421421.1:n.94+384_94+406delinsAT...
ENST00000509016.5:n.215+384_215+406delinsATATTCAGTCTCTAGAACTGAAC
ENST00000511552.5:n.480+384_480+406delinsATATTCAGTCTCTAGAACTGAAC
ENST00000513428.5:n.259+384_259+406delinsATATTCAGTCTCTAGAACTGAAC
ENST00000513523.1:n.262+384_262+406delinsATATTCAGTCTCTAGAACTGAAC
ENST00000513728.1:c.94+384_94+406delinsATATTCAGTCTCTAGAACTGAAC ENSP00000427135.1:n.94+384_94+406delinsAT...
ENST00000515017.5:c.94+384_94+406delinsATATTCAGTCTCTAGAACTGAAC ENSP00000424199.1:n.94+384_94+406delinsAT...
NM_001154.3:c.94+384_94+406delinsATATTCAGTCTCTAGAACTGAAC NP_001145.1:n.94+384_94+406delinsATATTCAG...
XM_017008141.2:c.94+384_94+406delinsATATTCAGTCTCTAGAACTGAAC XP_016863630.1:n.94+384_94+406delinsATATT...
NM_001154.4:c.94+384_94+406delinsATATTCAGTCTCTAGAACTGAAC MANE Select NP_001145.1:n.94+384_94+406delinsATATTCAG...