Canonical Allele Identifier: CA786352691

Gene: ANXA5

Linked Data

• dbSNP Id: rs1477827687
• gnomAD v3: 4-121685831-CACAGGTGAGGGTG-C
• gnomAD v4: 4-121685831-CACAGGTGAGGGTG-C
• MyVariant Identifiers: chr4:g.122606987_122606999del (hg19) ; chr4:g.121685832_121685844del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121685835_121685847del , CM000666.2:g.121685835_121685847del	GRCh38
NC_000004.11:g.122606990_122607002del , CM000666.1:g.122606990_122607002del	GRCh37
NC_000004.10:g.122826440_122826452del	NCBI36
NG_032042.1:g.16149_16161del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.94+444_94+456del MANE Select	ENSP00000296511.5:n.94+444_94+456del
ENST00000296511.9:c.94+444_94+456del	ENSP00000296511.5:n.94+444_94+456del
ENST00000501272.6:c.10-2367_10-2355del	ENSP00000424106.1:n.10-2367_10-2355del
ENST00000506395.5:c.94+444_94+456del	ENSP00000421421.1:n.94+444_94+456del
ENST00000509016.5:n.215+444_215+456del
ENST00000511552.5:n.480+444_480+456del
ENST00000513428.5:n.259+444_259+456del
ENST00000513523.1:n.262+444_262+456del
ENST00000513728.1:c.94+444_94+456del	ENSP00000427135.1:n.94+444_94+456del
ENST00000515017.5:c.94+444_94+456del	ENSP00000424199.1:n.94+444_94+456del
NM_001154.3:c.94+444_94+456del	NP_001145.1:n.94+444_94+456del
XM_017008141.2:c.94+444_94+456del	XP_016863630.1:n.94+444_94+456del
NM_001154.4:c.94+444_94+456del MANE Select	NP_001145.1:n.94+444_94+456del