Canonical Allele Identifier: CA1511397909

Gene: ANXA10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165522G= , CM000666.2:g.168165522G=	GRCh38
NC_000004.11:g.169086673G= , CM000666.1:g.169086673G=	GRCh37
NC_000004.10:g.169323248G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+196G= MANE Select	ENSP00000352248.3:n.480+196G=
ENST00000359299.7:c.480+196G=	ENSP00000352248.3:n.480+196G=
ENST00000503003.1:n.86+196G=
ENST00000507278.5:n.143+196G=
ENST00000617524.1:c.477+196G=	ENSP00000483710.1:n.477+196G=
NM_007193.4:c.480+196G=	NP_009124.2:n.480+196G=
XM_011531571.1:c.540+196G=	XP_011529873.1:n.540+196G=
XM_011531571.2:c.540+196G=	XP_011529873.1:n.540+196G=
NM_007193.5:c.480+196G= MANE Select	NP_009124.2:n.480+196G=