Canonical Allele Identifier: CA790668050

Gene: ANXA10

Linked Data

• dbSNP Id: rs1243924488
• gnomAD v3: 4-168165557-ATCTAT-A
• gnomAD v4: 4-168165557-ATCTAT-A
• MyVariant Identifiers: chr4:g.169086709_169086713del (hg19) ; chr4:g.168165558_168165562del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165562_168165566del , CM000666.2:g.168165562_168165566del	GRCh38
NC_000004.11:g.169086713_169086717del , CM000666.1:g.169086713_169086717del	GRCh37
NC_000004.10:g.169323288_169323292del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+236_480+240del MANE Select	ENSP00000352248.3:n.480+236_480+240del
ENST00000359299.7:c.480+236_480+240del	ENSP00000352248.3:n.480+236_480+240del
ENST00000503003.1:n.86+236_86+240del
ENST00000507278.5:n.143+236_143+240del
ENST00000617524.1:c.477+236_477+240del	ENSP00000483710.1:n.477+236_477+240del
NM_007193.4:c.480+236_480+240del	NP_009124.2:n.480+236_480+240del
XM_011531571.1:c.540+236_540+240del	XP_011529873.1:n.540+236_540+240del
XM_011531571.2:c.540+236_540+240del	XP_011529873.1:n.540+236_540+240del
NM_007193.5:c.480+236_480+240del MANE Select	NP_009124.2:n.480+236_480+240del