Canonical Allele Identifier: CA2671937247

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121686430-AAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686434_121686435del , CM000666.2:g.121686434_121686435del	GRCh38
NC_000004.11:g.122607589_122607590del , CM000666.1:g.122607589_122607590del	GRCh37
NC_000004.10:g.122827039_122827040del	NCBI36
NG_032042.1:g.15561_15562del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-60_10-59del MANE Select	ENSP00000296511.5:n.10-60_10-59del
ENST00000296511.9:c.10-60_10-59del	ENSP00000296511.5:n.10-60_10-59del
ENST00000501272.6:c.10-2955_10-2954del	ENSP00000424106.1:n.10-2955_10-2954del
ENST00000506395.5:c.10-60_10-59del	ENSP00000421421.1:n.10-60_10-59del
ENST00000509016.5:n.131-60_131-59del
ENST00000511552.5:n.396-60_396-59del
ENST00000513428.5:n.175-60_175-59del
ENST00000513523.1:n.178-60_178-59del
ENST00000513728.1:c.10-60_10-59del	ENSP00000427135.1:n.10-60_10-59del
ENST00000515017.5:c.10-60_10-59del	ENSP00000424199.1:n.10-60_10-59del
NM_001154.3:c.10-60_10-59del	NP_001145.1:n.10-60_10-59del
XM_017008141.2:c.10-60_10-59del	XP_016863630.1:n.10-60_10-59del
NM_001154.4:c.10-60_10-59del MANE Select	NP_001145.1:n.10-60_10-59del