Canonical Allele Identifier: CA555999447

Gene: ANXA10

Linked Data

• dbSNP Id: rs1370271378
• gnomAD v2: 4-169086562-ACAG-A
• gnomAD v3: 4-168165411-ACAG-A
• gnomAD v4: 4-168165411-ACAG-A
• MyVariant Identifiers: chr4:g.169086563_169086565del (hg19) ; chr4:g.168165412_168165414del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165412_168165414del , CM000666.2:g.168165412_168165414del	GRCh38
NC_000004.11:g.169086563_169086565del , CM000666.1:g.169086563_169086565del	GRCh37
NC_000004.10:g.169323138_169323140del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+86_480+88del MANE Select	ENSP00000352248.3:n.480+86_480+88del
ENST00000359299.7:c.480+86_480+88del	ENSP00000352248.3:n.480+86_480+88del
ENST00000503003.1:n.86+86_86+88del
ENST00000507278.5:n.143+86_143+88del
ENST00000617524.1:c.477+86_477+88del	ENSP00000483710.1:n.477+86_477+88del
NM_007193.4:c.480+86_480+88del	NP_009124.2:n.480+86_480+88del
XM_011531571.1:c.540+86_540+88del	XP_011529873.1:n.540+86_540+88del
XM_011531571.2:c.540+86_540+88del	XP_011529873.1:n.540+86_540+88del
NM_007193.5:c.480+86_480+88del MANE Select	NP_009124.2:n.480+86_480+88del