Canonical Allele Identifier: CA555999457

Gene: ANXA10

Linked Data

• dbSNP Id: rs1441381305
• gnomAD v2: 4-169086680-CCTCAA-C
• gnomAD v3: 4-168165529-CCTCAA-C
• gnomAD v4: 4-168165529-CCTCAA-C
• MyVariant Identifiers: chr4:g.169086681_169086685del (hg19) ; chr4:g.168165530_168165534del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165533_168165537del , CM000666.2:g.168165533_168165537del	GRCh38
NC_000004.11:g.169086684_169086688del , CM000666.1:g.169086684_169086688del	GRCh37
NC_000004.10:g.169323259_169323263del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+207_480+211del MANE Select	ENSP00000352248.3:n.480+207_480+211del
ENST00000359299.7:c.480+207_480+211del	ENSP00000352248.3:n.480+207_480+211del
ENST00000503003.1:n.86+207_86+211del
ENST00000507278.5:n.143+207_143+211del
ENST00000617524.1:c.477+207_477+211del	ENSP00000483710.1:n.477+207_477+211del
NM_007193.4:c.480+207_480+211del	NP_009124.2:n.480+207_480+211del
XM_011531571.1:c.540+207_540+211del	XP_011529873.1:n.540+207_540+211del
XM_011531571.2:c.540+207_540+211del	XP_011529873.1:n.540+207_540+211del
NM_007193.5:c.480+207_480+211del MANE Select	NP_009124.2:n.480+207_480+211del