Canonical Allele Identifier: CA3007293319

Gene: ANXA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.69788031del , CM000664.2:g.69788031del	GRCh38
NC_000002.11:g.70015163del , CM000664.1:g.70015163del	GRCh37
NC_000002.10:g.69868667del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394295.6:c.10-23del MANE Select	ENSP00000377833.4:n.10-23del
ENST00000394295.5:c.10-23del	ENSP00000377833.4:n.10-23del
ENST00000409920.5:c.10-23del	ENSP00000386756.1:n.10-23del
ENST00000460439.5:n.156-23del
ENST00000460942.5:n.126+6457del
ENST00000477632.5:n.137-23del
ENST00000484219.1:n.194-23del
ENST00000487351.6:n.99-23del
ENST00000635311.1:c.10-23del	ENSP00000489316.1:n.10-23del
NM_001153.3:c.10-23del	NP_001144.1:n.10-23del
XM_011532805.1:c.10-23del	XP_011531107.1:n.10-23del
NM_001153.4:c.10-23del	NP_001144.1:n.10-23del
NM_001320698.1:c.10-23del	NP_001307627.1:n.10-23del
NM_001320700.1:c.10-23del	NP_001307629.1:n.10-23del
NM_001320702.1:c.-279+6457del	NP_001307631.1:n.-279+6457del
NM_001365496.1:c.10-23del	NP_001352425.1:n.10-23del
XM_017003943.1:c.10-23del	XP_016859432.1:n.10-23del
XM_017003944.1:c.-366-23del	XP_016859433.1:n.-366-23del
XM_024452834.1:c.10-23del	XP_024308602.1:n.10-23del
XM_024452835.1:c.10-23del	XP_024308603.1:n.10-23del
XR_001738734.2:n.129-23del
NM_001153.5:c.10-23del MANE Select	NP_001144.1:n.10-23del
NM_001320698.2:c.10-23del	NP_001307627.1:n.10-23del
NM_001320700.2:c.10-23del	NP_001307629.1:n.10-23del
NM_001320702.2:c.-279+6457del	NP_001307631.1:n.-279+6457del
NM_001365496.2:c.10-23del	NP_001352425.1:n.10-23del