Canonical Allele Identifier: CA790668034

Gene: ANXA10

Linked Data

• dbSNP Id: rs1330872874
• gnomAD v3: 4-168165537-C-CTA
• gnomAD v4: 4-168165537-C-CTA
• MyVariant Identifiers: chr4:g.169086688_169086689insTA (hg19) ; chr4:g.168165537_168165538insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165539_168165540dup , CM000666.2:g.168165539_168165540dup	GRCh38
NC_000004.11:g.169086690_169086691dup , CM000666.1:g.169086690_169086691dup	GRCh37
NC_000004.10:g.169323265_169323266dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+213_480+214dup MANE Select	ENSP00000352248.3:n.480+213_480+214dup
ENST00000359299.7:c.480+213_480+214dup	ENSP00000352248.3:n.480+213_480+214dup
ENST00000503003.1:n.86+213_86+214dup
ENST00000507278.5:n.143+213_143+214dup
ENST00000617524.1:c.477+213_477+214dup	ENSP00000483710.1:n.477+213_477+214dup
NM_007193.4:c.480+213_480+214dup	NP_009124.2:n.480+213_480+214dup
XM_011531571.1:c.540+213_540+214dup	XP_011529873.1:n.540+213_540+214dup
XM_011531571.2:c.540+213_540+214dup	XP_011529873.1:n.540+213_540+214dup
NM_007193.5:c.480+213_480+214dup MANE Select	NP_009124.2:n.480+213_480+214dup