Canonical Allele Identifier: CA104731451

Gene: ANXA5

Linked Data

• dbSNP Id: rs1131239
• MyVariant Identifiers: chr4:g.121696590G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696590G>C , CM000666.2:g.121696590G>C	GRCh38
NC_000004.11:g.122617745G>C , CM000666.1:g.122617745G>C	GRCh37
NC_000004.10:g.122837195G>C	NCBI36
NG_032042.1:g.5403C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.-1C>G MANE Select	ENSP00000296511.5:n.-1C>G
ENST00000296511.9:c.-1C>G	ENSP00000296511.5:n.-1C>G
ENST00000501272.6:c.-1C>G	ENSP00000424106.1:n.-1C>G
ENST00000506395.5:c.-1C>G	ENSP00000421421.1:n.-1C>G
ENST00000509016.5:n.130+273C>G
ENST00000511552.5:n.386C>G
ENST00000513428.5:n.165C>G
ENST00000513523.1:n.168C>G
ENST00000513728.1:c.-1C>G	ENSP00000427135.1:n.-1C>G
ENST00000515017.5:c.-1C>G	ENSP00000424199.1:n.-1C>G
NM_001154.3:c.-1C>G	NP_001145.1:n.-1C>G
XM_017008141.2:c.-1C>G	XP_016863630.1:n.-1C>G
NM_001154.4:c.-1C>G MANE Select	NP_001145.1:n.-1C>G