Canonical Allele Identifier: CA554174466

Gene: ANXA5

Linked Data

• dbSNP Id: rs1368203290
• gnomAD v2: 4-122607531-ATTCACGAAACACAG-A
• gnomAD v4: 4-121686376-ATTCACGAAACACAG-A
• MyVariant Identifiers: chr4:g.122607532_122607545del (hg19) ; chr4:g.121686377_121686390del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686378_121686391del , CM000666.2:g.121686378_121686391del	GRCh38
NC_000004.11:g.122607533_122607546del , CM000666.1:g.122607533_122607546del	GRCh37
NC_000004.10:g.122826983_122826996del	NCBI36
NG_032042.1:g.15603_15616del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-18_10-5del MANE Select	ENSP00000296511.5:n.10-18_10-5del
ENST00000296511.9:c.10-18_10-5del	ENSP00000296511.5:n.10-18_10-5del
ENST00000501272.6:c.10-2913_10-2900del	ENSP00000424106.1:n.10-2913_10-2900del
ENST00000506395.5:c.10-18_10-5del	ENSP00000421421.1:n.10-18_10-5del
ENST00000509016.5:n.131-18_131-5del
ENST00000511552.5:n.396-18_396-5del
ENST00000513428.5:n.175-18_175-5del
ENST00000513523.1:n.178-18_178-5del
ENST00000513728.1:c.10-18_10-5del	ENSP00000427135.1:n.10-18_10-5del
ENST00000515017.5:c.10-18_10-5del	ENSP00000424199.1:n.10-18_10-5del
NM_001154.3:c.10-18_10-5del	NP_001145.1:n.10-18_10-5del
XM_017008141.2:c.10-18_10-5del	XP_016863630.1:n.10-18_10-5del
NM_001154.4:c.10-18_10-5del MANE Select	NP_001145.1:n.10-18_10-5del