Canonical Allele Identifier: CA2671937995

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121696879-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696879A>C , CM000666.2:g.121696879A>C	GRCh38
NC_000004.11:g.122618034A>C , CM000666.1:g.122618034A>C	GRCh37
NC_000004.10:g.122837484A>C	NCBI36
NG_032042.1:g.5114T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.-52T>G MANE Select	ENSP00000296511.5:n.-52T>G
ENST00000296511.9:c.-52T>G	ENSP00000296511.5:n.-52T>G
ENST00000501272.6:c.-52T>G	ENSP00000424106.1:n.-52T>G
ENST00000506395.5:c.-52T>G	ENSP00000421421.1:n.-52T>G
ENST00000509016.5:n.114T>G
ENST00000511552.5:n.97T>G
ENST00000513428.5:n.114T>G
ENST00000513523.1:n.117T>G
ENST00000513728.1:c.-52T>G	ENSP00000427135.1:n.-52T>G
ENST00000515017.5:c.-52T>G	ENSP00000424199.1:n.-52T>G
NM_001154.3:c.-52T>G	NP_001145.1:n.-52T>G
XM_017008141.2:c.-52T>G	XP_016863630.1:n.-52T>G
NM_001154.4:c.-52T>G MANE Select	NP_001145.1:n.-52T>G