Canonical Allele Identifier: CA2671938105

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121696961-C-CTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696961_121696962insTGG , CM000666.2:g.121696961_121696962insTGG	GRCh38
NC_000004.11:g.122618116_122618117insTGG , CM000666.1:g.122618116_122618117insTGG	GRCh37
NC_000004.10:g.122837566_122837567insTGG	NCBI36
NG_032042.1:g.5031_5032insCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.-135_-134insCCA MANE Select	ENSP00000296511.5:n.-135_-134insCCA
ENST00000296511.9:c.-135_-134insCCA	ENSP00000296511.5:n.-135_-134insCCA
ENST00000501272.6:c.-135_-134insCCA	ENSP00000424106.1:n.-135_-134insCCA
ENST00000506395.5:c.-135_-134insCCA	ENSP00000421421.1:n.-135_-134insCCA
ENST00000509016.5:n.31_32insCCA
ENST00000511552.5:n.14_15insCCA
ENST00000513428.5:n.31_32insCCA
ENST00000513523.1:n.34_35insCCA
ENST00000513728.1:c.-135_-134insCCA	ENSP00000427135.1:n.-135_-134insCCA
ENST00000515017.5:c.-135_-134insCCA	ENSP00000424199.1:n.-135_-134insCCA
NM_001154.3:c.-135_-134insCCA	NP_001145.1:n.-135_-134insCCA
XM_017008141.2:c.-135_-134insCCA	XP_016863630.1:n.-135_-134insCCA
NM_001154.4:c.-135_-134insCCA MANE Select	NP_001145.1:n.-135_-134insCCA