Canonical Allele Identifier: CA790668088

Gene: ANXA10

Linked Data

• dbSNP Id: rs1293346134
• gnomAD v3: 4-168165593-ATAAT-A
• gnomAD v4: 4-168165593-ATAAT-A
• MyVariant Identifiers: chr4:g.169086745_169086748del (hg19) ; chr4:g.168165594_168165597del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165599_168165602del , CM000666.2:g.168165599_168165602del	GRCh38
NC_000004.11:g.169086750_169086753del , CM000666.1:g.169086750_169086753del	GRCh37
NC_000004.10:g.169323325_169323328del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+273_480+276del MANE Select	ENSP00000352248.3:n.480+273_480+276del
ENST00000359299.7:c.480+273_480+276del	ENSP00000352248.3:n.480+273_480+276del
ENST00000503003.1:n.86+273_86+276del
ENST00000507278.5:n.143+273_143+276del
ENST00000617524.1:c.477+273_477+276del	ENSP00000483710.1:n.477+273_477+276del
NM_007193.4:c.480+273_480+276del	NP_009124.2:n.480+273_480+276del
XM_011531571.1:c.540+273_540+276del	XP_011529873.1:n.540+273_540+276del
XM_011531571.2:c.540+273_540+276del	XP_011529873.1:n.540+273_540+276del
NM_007193.5:c.480+273_480+276del MANE Select	NP_009124.2:n.480+273_480+276del