Canonical Allele Identifier: CA2739866752
Gene: ANXA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151100916A>C , CM000667.2:g.151100916A>C GRCh38
NC_000005.9:g.150480477A>C , CM000667.1:g.150480477A>C GRCh37
NC_000005.8:g.150460670A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*532T>G MANE Select ENSP00000346550.5:n.*532T>G
ENST00000522664.5:c.247T>G
NM_001155.4:c.*532T>G NP_001146.2:n.*532T>G
NM_001193544.1:c.*532T>G NP_001180473.1:n.*532T>G
NM_001363114.1:c.*532T>G NP_001350043.1:n.*532T>G
NM_001155.5:c.*532T>G MANE Select NP_001146.2:n.*532T>G
NM_001193544.2:c.*532T>G NP_001180473.1:n.*532T>G
NM_001363114.2:c.*532T>G NP_001350043.1:n.*532T>G