Canonical Allele Identifier: CA129882780
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs747437386
gnomAD v2: 5-150480635-A-AC
gnomAD v3: 5-151101074-A-AC
gnomAD v4: 5-151101074-A-AC
MyVariant Identifiers: chr5:g.150480635_150480636insC (hg19) chr5:g.151101074_151101075insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151101079dup , CM000667.2:g.151101079dup GRCh38
NC_000005.9:g.150480640dup , CM000667.1:g.150480640dup GRCh37
NC_000005.8:g.150460833dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*373dup MANE Select ENSP00000346550.5:n.*373dup
ENST00000522664.5:c.201-113dup
NM_001155.4:c.*373dup NP_001146.2:n.*373dup
NM_001193544.1:c.*373dup NP_001180473.1:n.*373dup
NM_001363114.1:c.*373dup NP_001350043.1:n.*373dup
NM_001155.5:c.*373dup MANE Select NP_001146.2:n.*373dup
NM_001193544.2:c.*373dup NP_001180473.1:n.*373dup
NM_001363114.2:c.*373dup NP_001350043.1:n.*373dup
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