Canonical Allele Identifier: CA790668072

Gene: ANXA10

Linked Data

• dbSNP Id: rs1364630288
• gnomAD v3: 4-168165574-TATAA-T
• gnomAD v4: 4-168165574-TATAA-T
• MyVariant Identifiers: chr4:g.169086726_169086729del (hg19) ; chr4:g.168165575_168165578del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165578_168165581del , CM000666.2:g.168165578_168165581del	GRCh38
NC_000004.11:g.169086729_169086732del , CM000666.1:g.169086729_169086732del	GRCh37
NC_000004.10:g.169323304_169323307del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+252_480+255del MANE Select	ENSP00000352248.3:n.480+252_480+255del
ENST00000359299.7:c.480+252_480+255del	ENSP00000352248.3:n.480+252_480+255del
ENST00000503003.1:n.86+252_86+255del
ENST00000507278.5:n.143+252_143+255del
ENST00000617524.1:c.477+252_477+255del	ENSP00000483710.1:n.477+252_477+255del
NM_007193.4:c.480+252_480+255del	NP_009124.2:n.480+252_480+255del
XM_011531571.1:c.540+252_540+255del	XP_011529873.1:n.540+252_540+255del
XM_011531571.2:c.540+252_540+255del	XP_011529873.1:n.540+252_540+255del
NM_007193.5:c.480+252_480+255del MANE Select	NP_009124.2:n.480+252_480+255del