Canonical Allele Identifier: CA104723160

Gene: ANXA5

Linked Data

• dbSNP Id: rs992619586
• gnomAD v3: 4-121686041-T-TG
• gnomAD v4: 4-121686041-T-TG
• MyVariant Identifiers: chr4:g.122607196_122607197insG (hg19) ; chr4:g.121686041_121686042insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686041_121686042insG , CM000666.2:g.121686041_121686042insG	GRCh38
NC_000004.11:g.122607196_122607197insG , CM000666.1:g.122607196_122607197insG	GRCh37
NC_000004.10:g.122826646_122826647insG	NCBI36
NG_032042.1:g.15951_15952insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.94+246_94+247insC MANE Select	ENSP00000296511.5:n.94+246_94+247insC
ENST00000296511.9:c.94+246_94+247insC	ENSP00000296511.5:n.94+246_94+247insC
ENST00000501272.6:c.10-2565_10-2564insC	ENSP00000424106.1:n.10-2565_10-2564insC
ENST00000506395.5:c.94+246_94+247insC	ENSP00000421421.1:n.94+246_94+247insC
ENST00000509016.5:n.215+246_215+247insC
ENST00000511552.5:n.480+246_480+247insC
ENST00000513428.5:n.259+246_259+247insC
ENST00000513523.1:n.262+246_262+247insC
ENST00000513728.1:c.94+246_94+247insC	ENSP00000427135.1:n.94+246_94+247insC
ENST00000515017.5:c.94+246_94+247insC	ENSP00000424199.1:n.94+246_94+247insC
NM_001154.3:c.94+246_94+247insC	NP_001145.1:n.94+246_94+247insC
XM_017008141.2:c.94+246_94+247insC	XP_016863630.1:n.94+246_94+247insC
NM_001154.4:c.94+246_94+247insC MANE Select	NP_001145.1:n.94+246_94+247insC