Canonical Allele Identifier: CA786352750

Gene: ANXA5

Linked Data

• dbSNP Id: rs1465842910
• gnomAD v3: 4-121685921-C-CA
• gnomAD v4: 4-121685921-C-CA
• MyVariant Identifiers: chr4:g.122607076_122607077insA (hg19) ; chr4:g.121685921_121685922insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121685923dup , CM000666.2:g.121685923dup	GRCh38
NC_000004.11:g.122607078dup , CM000666.1:g.122607078dup	GRCh37
NC_000004.10:g.122826528dup	NCBI36
NG_032042.1:g.16071dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000296511.10:c.94+366dup MANE Select	ENSP00000296511.5:n.94+366dup
ENST00000296511.9:c.94+366dup	ENSP00000296511.5:n.94+366dup
ENST00000501272.6:c.10-2445dup	ENSP00000424106.1:n.10-2445dup
ENST00000506395.5:c.94+366dup	ENSP00000421421.1:n.94+366dup
ENST00000509016.5:n.215+366dup
ENST00000511552.5:n.480+366dup
ENST00000513428.5:n.259+366dup
ENST00000513523.1:n.262+366dup
ENST00000513728.1:c.94+366dup	ENSP00000427135.1:n.94+366dup
ENST00000515017.5:c.94+366dup	ENSP00000424199.1:n.94+366dup
NM_001154.3:c.94+366dup	NP_001145.1:n.94+366dup
XM_017008141.2:c.94+366dup	XP_016863630.1:n.94+366dup
NM_001154.4:c.94+366dup MANE Select	NP_001145.1:n.94+366dup