Canonical Allele Identifier: CA1489952246

Gene: ANXA5

Linked Data

• dbSNP Id: rs1724892123

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686442_121686444del , CM000666.2:g.121686442_121686444del	GRCh38
NC_000004.11:g.122607597_122607599del , CM000666.1:g.122607597_122607599del	GRCh37
NC_000004.10:g.122827047_122827049del	NCBI36
NG_032042.1:g.15550_15552del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-71_10-69del MANE Select	ENSP00000296511.5:n.10-71_10-69del
ENST00000296511.9:c.10-71_10-69del	ENSP00000296511.5:n.10-71_10-69del
ENST00000501272.6:c.10-2966_10-2964del	ENSP00000424106.1:n.10-2966_10-2964del
ENST00000506395.5:c.10-71_10-69del	ENSP00000421421.1:n.10-71_10-69del
ENST00000509016.5:n.131-71_131-69del
ENST00000511552.5:n.396-71_396-69del
ENST00000513428.5:n.175-71_175-69del
ENST00000513523.1:n.178-71_178-69del
ENST00000513728.1:c.10-71_10-69del	ENSP00000427135.1:n.10-71_10-69del
ENST00000515017.5:c.10-71_10-69del	ENSP00000424199.1:n.10-71_10-69del
NM_001154.3:c.10-71_10-69del	NP_001145.1:n.10-71_10-69del
XM_017008141.2:c.10-71_10-69del	XP_016863630.1:n.10-71_10-69del
NM_001154.4:c.10-71_10-69del MANE Select	NP_001145.1:n.10-71_10-69del