Canonical Allele Identifier: CA2671937234

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121686397-T-TATTC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686400_121686403dup , CM000666.2:g.121686400_121686403dup	GRCh38
NC_000004.11:g.122607555_122607558dup , CM000666.1:g.122607555_122607558dup	GRCh37
NC_000004.10:g.122827005_122827008dup	NCBI36
NG_032042.1:g.15592_15595dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-29_10-26dup MANE Select	ENSP00000296511.5:n.10-29_10-26dup
ENST00000296511.9:c.10-29_10-26dup	ENSP00000296511.5:n.10-29_10-26dup
ENST00000501272.6:c.10-2924_10-2921dup	ENSP00000424106.1:n.10-2924_10-2921dup
ENST00000506395.5:c.10-29_10-26dup	ENSP00000421421.1:n.10-29_10-26dup
ENST00000509016.5:n.131-29_131-26dup
ENST00000511552.5:n.396-29_396-26dup
ENST00000513428.5:n.175-29_175-26dup
ENST00000513523.1:n.178-29_178-26dup
ENST00000513728.1:c.10-29_10-26dup	ENSP00000427135.1:n.10-29_10-26dup
ENST00000515017.5:c.10-29_10-26dup	ENSP00000424199.1:n.10-29_10-26dup
NM_001154.3:c.10-29_10-26dup	NP_001145.1:n.10-29_10-26dup
XM_017008141.2:c.10-29_10-26dup	XP_016863630.1:n.10-29_10-26dup
NM_001154.4:c.10-29_10-26dup MANE Select	NP_001145.1:n.10-29_10-26dup