Canonical Allele Identifier: CA790668021

Gene: ANXA10

Linked Data

• dbSNP Id: rs1253419324
• gnomAD v3: 4-168165514-C-T
• gnomAD v4: 4-168165514-C-T
• MyVariant Identifiers: chr4:g.169086665C>T (hg19) ; chr4:g.168165514C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168165514C>T , CM000666.2:g.168165514C>T	GRCh38
NC_000004.11:g.169086665C>T , CM000666.1:g.169086665C>T	GRCh37
NC_000004.10:g.169323240C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359299.8:c.480+188C>T MANE Select	ENSP00000352248.3:n.480+188C>T
ENST00000359299.7:c.480+188C>T	ENSP00000352248.3:n.480+188C>T
ENST00000503003.1:n.86+188C>T
ENST00000507278.5:n.143+188C>T
ENST00000617524.1:c.477+188C>T	ENSP00000483710.1:n.477+188C>T
NM_007193.4:c.480+188C>T	NP_009124.2:n.480+188C>T
XM_011531571.1:c.540+188C>T	XP_011529873.1:n.540+188C>T
XM_011531571.2:c.540+188C>T	XP_011529873.1:n.540+188C>T
NM_007193.5:c.480+188C>T MANE Select	NP_009124.2:n.480+188C>T