Canonical Allele Identifier: CA104723104

Gene: ANXA5

Linked Data

• dbSNP Id: rs113259484
• MyVariant Identifiers: chr4:g.122607177_122607178insC (hg19) ; chr4:g.121686022_121686023insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686022_121686023insC , CM000666.2:g.121686022_121686023insC	GRCh38
NC_000004.11:g.122607177_122607178insC , CM000666.1:g.122607177_122607178insC	GRCh37
NC_000004.10:g.122826627_122826628insC	NCBI36
NG_032042.1:g.15970_15971insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.94+265_94+266insG MANE Select	ENSP00000296511.5:n.94+265_94+266insG
ENST00000296511.9:c.94+265_94+266insG	ENSP00000296511.5:n.94+265_94+266insG
ENST00000501272.6:c.10-2546_10-2545insG	ENSP00000424106.1:n.10-2546_10-2545insG
ENST00000506395.5:c.94+265_94+266insG	ENSP00000421421.1:n.94+265_94+266insG
ENST00000509016.5:n.215+265_215+266insG
ENST00000511552.5:n.480+265_480+266insG
ENST00000513428.5:n.259+265_259+266insG
ENST00000513523.1:n.262+265_262+266insG
ENST00000513728.1:c.94+265_94+266insG	ENSP00000427135.1:n.94+265_94+266insG
ENST00000515017.5:c.94+265_94+266insG	ENSP00000424199.1:n.94+265_94+266insG
NM_001154.3:c.94+265_94+266insG	NP_001145.1:n.94+265_94+266insG
XM_017008141.2:c.94+265_94+266insG	XP_016863630.1:n.94+265_94+266insG
NM_001154.4:c.94+265_94+266insG MANE Select	NP_001145.1:n.94+265_94+266insG