Canonical Allele Identifier: CA2671937244

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121686420-CAAAGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686424_121686428del , CM000666.2:g.121686424_121686428del	GRCh38
NC_000004.11:g.122607579_122607583del , CM000666.1:g.122607579_122607583del	GRCh37
NC_000004.10:g.122827029_122827033del	NCBI36
NG_032042.1:g.15568_15572del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-53_10-49del MANE Select	ENSP00000296511.5:n.10-53_10-49del
ENST00000296511.9:c.10-53_10-49del	ENSP00000296511.5:n.10-53_10-49del
ENST00000501272.6:c.10-2948_10-2944del	ENSP00000424106.1:n.10-2948_10-2944del
ENST00000506395.5:c.10-53_10-49del	ENSP00000421421.1:n.10-53_10-49del
ENST00000509016.5:n.131-53_131-49del
ENST00000511552.5:n.396-53_396-49del
ENST00000513428.5:n.175-53_175-49del
ENST00000513523.1:n.178-53_178-49del
ENST00000513728.1:c.10-53_10-49del	ENSP00000427135.1:n.10-53_10-49del
ENST00000515017.5:c.10-53_10-49del	ENSP00000424199.1:n.10-53_10-49del
NM_001154.3:c.10-53_10-49del	NP_001145.1:n.10-53_10-49del
XM_017008141.2:c.10-53_10-49del	XP_016863630.1:n.10-53_10-49del
NM_001154.4:c.10-53_10-49del MANE Select	NP_001145.1:n.10-53_10-49del