Canonical Allele Identifier: CA1067436737

Gene: ANXA5

Linked Data

• dbSNP Id: rs1725091520
• gnomAD v3: 4-121696763-ACCGGGACAGCTCTCGGCCGAGCGTCCGCGCGAATCCAGTGCCCCGCGACCACGCTCTCCTCTCCAGAAGGAGCCCCCTCC-A
• gnomAD v4: 4-121696763-ACCGGGACAGCTCTCGGCCGAGCGTCCGCGCGAATCCAGTGCCCCGCGACCACGCTCTCCTCTCCAGAAGGAGCCCCCTCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696769_121696848del , CM000666.2:g.121696769_121696848del	GRCh38
NC_000004.11:g.122617924_122618003del , CM000666.1:g.122617924_122618003del	GRCh37
NC_000004.10:g.122837374_122837453del	NCBI36
NG_032042.1:g.5150_5229del

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.-36+20_-36+99del MANE Select	ENSP00000296511.5:n.-36+20_-36+99del
ENST00000296511.9:c.-36+20_-36+99del	ENSP00000296511.5:n.-36+20_-36+99del
ENST00000501272.6:c.-36+20_-36+99del	ENSP00000424106.1:n.-36+20_-36+99del
ENST00000506395.5:c.-36+20_-36+99del	ENSP00000421421.1:n.-36+20_-36+99del
ENST00000509016.5:n.130+20_130+99del
ENST00000511552.5:n.133_212del
ENST00000513428.5:n.130+20_130+99del
ENST00000513523.1:n.133+20_133+99del
ENST00000513728.1:c.-36+20_-36+99del	ENSP00000427135.1:n.-36+20_-36+99del
ENST00000515017.5:c.-36+20_-36+99del	ENSP00000424199.1:n.-36+20_-36+99del
NM_001154.3:c.-36+20_-36+99del	NP_001145.1:n.-36+20_-36+99del
XM_017008141.2:c.-36+20_-36+99del	XP_016863630.1:n.-36+20_-36+99del
NM_001154.4:c.-36+20_-36+99del MANE Select	NP_001145.1:n.-36+20_-36+99del