Canonical Allele Identifier: CA786356316

Gene: ANXA5

Linked Data

• dbSNP Id: rs1192673456
• gnomAD v3: 4-121693512-A-T
• gnomAD v4: 4-121693512-A-T
• MyVariant Identifiers: chr4:g.122614667A>T (hg19) ; chr4:g.121693512A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121693512A>T , CM000666.2:g.121693512A>T	GRCh38
NC_000004.11:g.122614667A>T , CM000666.1:g.122614667A>T	GRCh37
NC_000004.10:g.122834117A>T	NCBI36
NG_032042.1:g.8481T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.9+3069T>A MANE Select	ENSP00000296511.5:n.9+3069T>A
ENST00000296511.9:c.9+3069T>A	ENSP00000296511.5:n.9+3069T>A
ENST00000501272.6:c.9+3069T>A	ENSP00000424106.1:n.9+3069T>A
ENST00000506395.5:c.9+3069T>A	ENSP00000421421.1:n.9+3069T>A
ENST00000509016.5:n.130+3351T>A
ENST00000511552.5:n.395+3069T>A
ENST00000513428.5:n.174+3069T>A
ENST00000513523.1:n.177+3069T>A
ENST00000513728.1:c.9+3069T>A	ENSP00000427135.1:n.9+3069T>A
ENST00000515017.5:c.9+3069T>A	ENSP00000424199.1:n.9+3069T>A
NM_001154.3:c.9+3069T>A	NP_001145.1:n.9+3069T>A
XM_017008141.2:c.9+3069T>A	XP_016863630.1:n.9+3069T>A
NM_001154.4:c.9+3069T>A MANE Select	NP_001145.1:n.9+3069T>A