Canonical Allele Identifier: CA790668094

Gene: ANXA10

Linked Data

• dbSNP Id: rs1370683072
• gnomAD v3: 4-168165599-AATTT-A
• gnomAD v4: 4-168165599-AATTT-A
• MyVariant Identifiers: chr4:g.169086751_169086754del (hg19) ; chr4:g.168165600_168165603del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165600_168165603del , CM000666.2:g.168165600_168165603del	GRCh38
NC_000004.11:g.169086751_169086754del , CM000666.1:g.169086751_169086754del	GRCh37
NC_000004.10:g.169323326_169323329del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+274_480+277del MANE Select	ENSP00000352248.3:n.480+274_480+277del
ENST00000359299.7:c.480+274_480+277del	ENSP00000352248.3:n.480+274_480+277del
ENST00000503003.1:n.86+274_86+277del
ENST00000507278.5:n.143+274_143+277del
ENST00000617524.1:c.477+274_477+277del	ENSP00000483710.1:n.477+274_477+277del
NM_007193.4:c.480+274_480+277del	NP_009124.2:n.480+274_480+277del
XM_011531571.1:c.540+274_540+277del	XP_011529873.1:n.540+274_540+277del
XM_011531571.2:c.540+274_540+277del	XP_011529873.1:n.540+274_540+277del
NM_007193.5:c.480+274_480+277del MANE Select	NP_009124.2:n.480+274_480+277del