Canonical Allele Identifier: CA2671937913

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121696825-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696827del , CM000666.2:g.121696827del	GRCh38
NC_000004.11:g.122617982del , CM000666.1:g.122617982del	GRCh37
NC_000004.10:g.122837432del	NCBI36
NG_032042.1:g.5167del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.-36+37del MANE Select	ENSP00000296511.5:n.-36+37del
ENST00000296511.9:c.-36+37del	ENSP00000296511.5:n.-36+37del
ENST00000501272.6:c.-36+37del	ENSP00000424106.1:n.-36+37del
ENST00000506395.5:c.-36+37del	ENSP00000421421.1:n.-36+37del
ENST00000509016.5:n.130+37del
ENST00000511552.5:n.150del
ENST00000513428.5:n.130+37del
ENST00000513523.1:n.133+37del
ENST00000513728.1:c.-36+37del	ENSP00000427135.1:n.-36+37del
ENST00000515017.5:c.-36+37del	ENSP00000424199.1:n.-36+37del
NM_001154.3:c.-36+37del	NP_001145.1:n.-36+37del
XM_017008141.2:c.-36+37del	XP_016863630.1:n.-36+37del
NM_001154.4:c.-36+37del MANE Select	NP_001145.1:n.-36+37del