Canonical Allele Identifier: CA442057728

Gene: ANXA10

Linked Data

• dbSNP Id: rs1731859882
• gnomAD v2: 4-169086557-ATAG-A
• gnomAD v3: 4-168165406-ATAG-A
• gnomAD v4: 4-168165406-ATAG-A
• MyVariant Identifiers: chr4:g.169086558_169086560del (hg19) ; chr4:g.168165407_168165409del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165407_168165409del , CM000666.2:g.168165407_168165409del	GRCh38
NC_000004.11:g.169086558_169086560del , CM000666.1:g.169086558_169086560del	GRCh37
NC_000004.10:g.169323133_169323135del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+81_480+83del MANE Select	ENSP00000352248.3:n.480+81_480+83del
ENST00000359299.7:c.480+81_480+83del	ENSP00000352248.3:n.480+81_480+83del
ENST00000503003.1:n.86+81_86+83del
ENST00000507278.5:n.143+81_143+83del
ENST00000617524.1:c.477+81_477+83del	ENSP00000483710.1:n.477+81_477+83del
NM_007193.4:c.480+81_480+83del	NP_009124.2:n.480+81_480+83del
XM_011531571.1:c.540+81_540+83del	XP_011529873.1:n.540+81_540+83del
XM_011531571.2:c.540+81_540+83del	XP_011529873.1:n.540+81_540+83del
NM_007193.5:c.480+81_480+83del MANE Select	NP_009124.2:n.480+81_480+83del