Canonical Allele Identifier: CA554175843

Gene: ANXA5

Linked Data

• dbSNP Id: rs1433358956
• gnomAD v2: 4-122614560-T-TA
• gnomAD v3: 4-121693405-T-TA
• gnomAD v4: 4-121693405-T-TA
• MyVariant Identifiers: chr4:g.122614561_122614562insA (hg19) ; chr4:g.121693406_121693407insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121693411dup , CM000666.2:g.121693411dup	GRCh38
NC_000004.11:g.122614566dup , CM000666.1:g.122614566dup	GRCh37
NC_000004.10:g.122834016dup	NCBI36
NG_032042.1:g.8587dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.9+3175dup MANE Select	ENSP00000296511.5:n.9+3175dup
ENST00000296511.9:c.9+3175dup	ENSP00000296511.5:n.9+3175dup
ENST00000501272.6:c.9+3175dup	ENSP00000424106.1:n.9+3175dup
ENST00000506395.5:c.9+3175dup	ENSP00000421421.1:n.9+3175dup
ENST00000509016.5:n.130+3457dup
ENST00000511552.5:n.395+3175dup
ENST00000513428.5:n.174+3175dup
ENST00000513523.1:n.177+3175dup
ENST00000513728.1:c.9+3175dup	ENSP00000427135.1:n.9+3175dup
ENST00000515017.5:c.9+3175dup	ENSP00000424199.1:n.9+3175dup
NM_001154.3:c.9+3175dup	NP_001145.1:n.9+3175dup
XM_017008141.2:c.9+3175dup	XP_016863630.1:n.9+3175dup
NM_001154.4:c.9+3175dup MANE Select	NP_001145.1:n.9+3175dup