Canonical Allele Identifier: CA2671937238

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121686403-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686403_121686404insG , CM000666.2:g.121686403_121686404insG	GRCh38
NC_000004.11:g.122607558_122607559insG , CM000666.1:g.122607558_122607559insG	GRCh37
NC_000004.10:g.122827008_122827009insG	NCBI36
NG_032042.1:g.15589_15590insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.10-32_10-31insC MANE Select	ENSP00000296511.5:n.10-32_10-31insC
ENST00000296511.9:c.10-32_10-31insC	ENSP00000296511.5:n.10-32_10-31insC
ENST00000501272.6:c.10-2927_10-2926insC	ENSP00000424106.1:n.10-2927_10-2926insC
ENST00000506395.5:c.10-32_10-31insC	ENSP00000421421.1:n.10-32_10-31insC
ENST00000509016.5:n.131-32_131-31insC
ENST00000511552.5:n.396-32_396-31insC
ENST00000513428.5:n.175-32_175-31insC
ENST00000513523.1:n.178-32_178-31insC
ENST00000513728.1:c.10-32_10-31insC	ENSP00000427135.1:n.10-32_10-31insC
ENST00000515017.5:c.10-32_10-31insC	ENSP00000424199.1:n.10-32_10-31insC
NM_001154.3:c.10-32_10-31insC	NP_001145.1:n.10-32_10-31insC
XM_017008141.2:c.10-32_10-31insC	XP_016863630.1:n.10-32_10-31insC
NM_001154.4:c.10-32_10-31insC MANE Select	NP_001145.1:n.10-32_10-31insC