Canonical Allele Identifier: CA2671937270

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121686464-TTCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686465_121686467del , CM000666.2:g.121686465_121686467del	GRCh38
NC_000004.11:g.122607620_122607622del , CM000666.1:g.122607620_122607622del	GRCh37
NC_000004.10:g.122827070_122827072del	NCBI36
NG_032042.1:g.15526_15528del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-95_10-93del MANE Select	ENSP00000296511.5:n.10-95_10-93del
ENST00000296511.9:c.10-95_10-93del	ENSP00000296511.5:n.10-95_10-93del
ENST00000501272.6:c.10-2990_10-2988del	ENSP00000424106.1:n.10-2990_10-2988del
ENST00000506395.5:c.10-95_10-93del	ENSP00000421421.1:n.10-95_10-93del
ENST00000509016.5:n.131-95_131-93del
ENST00000511552.5:n.396-95_396-93del
ENST00000513428.5:n.175-95_175-93del
ENST00000513523.1:n.178-95_178-93del
ENST00000513728.1:c.10-95_10-93del	ENSP00000427135.1:n.10-95_10-93del
ENST00000515017.5:c.10-95_10-93del	ENSP00000424199.1:n.10-95_10-93del
NM_001154.3:c.10-95_10-93del	NP_001145.1:n.10-95_10-93del
XM_017008141.2:c.10-95_10-93del	XP_016863630.1:n.10-95_10-93del
NM_001154.4:c.10-95_10-93del MANE Select	NP_001145.1:n.10-95_10-93del