Canonical Allele Identifier: CA2671938008

Gene: ANXA5

Linked Data

• gnomAD v4: 4-121696886-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696886C>G , CM000666.2:g.121696886C>G	GRCh38
NC_000004.11:g.122618041C>G , CM000666.1:g.122618041C>G	GRCh37
NC_000004.10:g.122837491C>G	NCBI36
NG_032042.1:g.5107G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.-59G>C MANE Select	ENSP00000296511.5:n.-59G>C
ENST00000296511.9:c.-59G>C	ENSP00000296511.5:n.-59G>C
ENST00000501272.6:c.-59G>C	ENSP00000424106.1:n.-59G>C
ENST00000506395.5:c.-59G>C	ENSP00000421421.1:n.-59G>C
ENST00000509016.5:n.107G>C
ENST00000511552.5:n.90G>C
ENST00000513428.5:n.107G>C
ENST00000513523.1:n.110G>C
ENST00000513728.1:c.-59G>C	ENSP00000427135.1:n.-59G>C
ENST00000515017.5:c.-59G>C	ENSP00000424199.1:n.-59G>C
NM_001154.3:c.-59G>C	NP_001145.1:n.-59G>C
XM_017008141.2:c.-59G>C	XP_016863630.1:n.-59G>C
NM_001154.4:c.-59G>C MANE Select	NP_001145.1:n.-59G>C