Canonical Allele Identifier: CA1511397912

Gene: ANXA10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165529_168165534delinsCCTCAA , CM000666.2:g.168165529_168165534delinsCCTCAA	GRCh38
NC_000004.11:g.169086680_169086685delinsCCTCAA , CM000666.1:g.169086680_169086685delinsCCTCAA	GRCh37
NC_000004.10:g.169323255_169323260delinsCCTCAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+203_480+208delinsCCTCAA MANE Select	ENSP00000352248.3:n.480+203_480+208delinsCCTCAA
ENST00000359299.7:c.480+203_480+208delinsCCTCAA	ENSP00000352248.3:n.480+203_480+208delinsCCTCAA
ENST00000503003.1:n.86+203_86+208delinsCCTCAA
ENST00000507278.5:n.143+203_143+208delinsCCTCAA
ENST00000617524.1:c.477+203_477+208delinsCCTCAA	ENSP00000483710.1:n.477+203_477+208delinsCCTCAA
NM_007193.4:c.480+203_480+208delinsCCTCAA	NP_009124.2:n.480+203_480+208delinsCCTCAA
XM_011531571.1:c.540+203_540+208delinsCCTCAA	XP_011529873.1:n.540+203_540+208delinsCCTCAA
XM_011531571.2:c.540+203_540+208delinsCCTCAA	XP_011529873.1:n.540+203_540+208delinsCCTCAA
NM_007193.5:c.480+203_480+208delinsCCTCAA MANE Select	NP_009124.2:n.480+203_480+208delinsCCTCAA