Canonical Allele Identifier: CA1591240990
Gene: ANXA6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151100781A= , CM000667.2:g.151100781A= GRCh38
NC_000005.9:g.150480342A= , CM000667.1:g.150480342A= GRCh37
NC_000005.8:g.150460535A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*667T= MANE Select ENSP00000346550.5:n.*667T=
ENST00000522664.5:c.382T=
NM_001155.4:c.*667T= NP_001146.2:n.*667T=
NM_001193544.1:c.*667T= NP_001180473.1:n.*667T=
NM_001363114.1:c.*667T= NP_001350043.1:n.*667T=
NM_001155.5:c.*667T= MANE Select NP_001146.2:n.*667T=
NM_001193544.2:c.*667T= NP_001180473.1:n.*667T=
NM_001363114.2:c.*667T= NP_001350043.1:n.*667T=
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