Canonical Allele Identifier: CA2604058125

Gene: ANXA5

Linked Data

• dbSNP Id: rs2110487568
• gnomAD v3: 4-121685898-T-TGA
• gnomAD v4: 4-121685898-T-TGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121685899_121685900dup , CM000666.2:g.121685899_121685900dup	GRCh38
NC_000004.11:g.122607054_122607055dup , CM000666.1:g.122607054_122607055dup	GRCh37
NC_000004.10:g.122826504_122826505dup	NCBI36
NG_032042.1:g.16093_16094dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.94+388_94+389dup MANE Select	ENSP00000296511.5:n.94+388_94+389dup
ENST00000296511.9:c.94+388_94+389dup	ENSP00000296511.5:n.94+388_94+389dup
ENST00000501272.6:c.10-2423_10-2422dup	ENSP00000424106.1:n.10-2423_10-2422dup
ENST00000506395.5:c.94+388_94+389dup	ENSP00000421421.1:n.94+388_94+389dup
ENST00000509016.5:n.215+388_215+389dup
ENST00000511552.5:n.480+388_480+389dup
ENST00000513428.5:n.259+388_259+389dup
ENST00000513523.1:n.262+388_262+389dup
ENST00000513728.1:c.94+388_94+389dup	ENSP00000427135.1:n.94+388_94+389dup
ENST00000515017.5:c.94+388_94+389dup	ENSP00000424199.1:n.94+388_94+389dup
NM_001154.3:c.94+388_94+389dup	NP_001145.1:n.94+388_94+389dup
XM_017008141.2:c.94+388_94+389dup	XP_016863630.1:n.94+388_94+389dup
NM_001154.4:c.94+388_94+389dup MANE Select	NP_001145.1:n.94+388_94+389dup