Canonical Allele Identifier: CA790667902

Gene: ANXA10

Linked Data

• dbSNP Id: rs33925175
• gnomAD v3: 4-168165389-CAAAAAAA-C
• gnomAD v4: 4-168165389-CAAAAAAA-C
• MyVariant Identifiers: chr4:g.169086541_169086547del (hg19) ; chr4:g.168165390_168165396del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165400_168165406del , CM000666.2:g.168165400_168165406del	GRCh38
NC_000004.11:g.169086551_169086557del , CM000666.1:g.169086551_169086557del	GRCh37
NC_000004.10:g.169323126_169323132del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+74_480+80del MANE Select	ENSP00000352248.3:n.480+74_480+80del
ENST00000359299.7:c.480+74_480+80del	ENSP00000352248.3:n.480+74_480+80del
ENST00000503003.1:n.86+74_86+80del
ENST00000507278.5:n.143+74_143+80del
ENST00000617524.1:c.477+74_477+80del	ENSP00000483710.1:n.477+74_477+80del
NM_007193.4:c.480+74_480+80del	NP_009124.2:n.480+74_480+80del
XM_011531571.1:c.540+74_540+80del	XP_011529873.1:n.540+74_540+80del
XM_011531571.2:c.540+74_540+80del	XP_011529873.1:n.540+74_540+80del
NM_007193.5:c.480+74_480+80del MANE Select	NP_009124.2:n.480+74_480+80del