Canonical Allele Identifier: CA563603840
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs1401571874
gnomAD v2: 5-150480274-ATGTGTTTG-A
gnomAD v3: 5-151100713-ATGTGTTTG-A
gnomAD v4: 5-151100713-ATGTGTTTG-A
MyVariant Identifiers: chr5:g.150480275_150480282del (hg19) chr5:g.151100714_151100721del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151100717_151100724del , CM000667.2:g.151100717_151100724del GRCh38
NC_000005.9:g.150480278_150480285del , CM000667.1:g.150480278_150480285del GRCh37
NC_000005.8:g.150460471_150460478del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*727_*734del MANE Select ENSP00000346550.5:n.*727_*734del
ENST00000522664.5:c.442_449del
NM_001155.4:c.*727_*734del NP_001146.2:n.*727_*734del
NM_001193544.1:c.*727_*734del NP_001180473.1:n.*727_*734del
NM_001363114.1:c.*727_*734del NP_001350043.1:n.*727_*734del
NM_001155.5:c.*727_*734del MANE Select NP_001146.2:n.*727_*734del
NM_001193544.2:c.*727_*734del NP_001180473.1:n.*727_*734del
NM_001363114.2:c.*727_*734del NP_001350043.1:n.*727_*734del
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