Canonical Allele Identifier: CA1489956879

Gene: ANXA5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696831_121696832delinsAG , CM000666.2:g.121696831_121696832delinsAG	GRCh38
NC_000004.11:g.122617986_122617987delinsAG , CM000666.1:g.122617986_122617987delinsAG	GRCh37
NC_000004.10:g.122837436_122837437delinsAG	NCBI36
NG_032042.1:g.5161_5162delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.-36+31_-36+32delinsCT MANE Select	ENSP00000296511.5:n.-36+31_-36+32delinsCT
ENST00000296511.9:c.-36+31_-36+32delinsCT	ENSP00000296511.5:n.-36+31_-36+32delinsCT
ENST00000501272.6:c.-36+31_-36+32delinsCT	ENSP00000424106.1:n.-36+31_-36+32delinsCT
ENST00000506395.5:c.-36+31_-36+32delinsCT	ENSP00000421421.1:n.-36+31_-36+32delinsCT
ENST00000509016.5:n.130+31_130+32delinsCT
ENST00000511552.5:n.144_145delinsCT
ENST00000513428.5:n.130+31_130+32delinsCT
ENST00000513523.1:n.133+31_133+32delinsCT
ENST00000513728.1:c.-36+31_-36+32delinsCT	ENSP00000427135.1:n.-36+31_-36+32delinsCT
ENST00000515017.5:c.-36+31_-36+32delinsCT	ENSP00000424199.1:n.-36+31_-36+32delinsCT
NM_001154.3:c.-36+31_-36+32delinsCT	NP_001145.1:n.-36+31_-36+32delinsCT
XM_017008141.2:c.-36+31_-36+32delinsCT	XP_016863630.1:n.-36+31_-36+32delinsCT
NM_001154.4:c.-36+31_-36+32delinsCT MANE Select	NP_001145.1:n.-36+31_-36+32delinsCT