Canonical Allele Identifier: CA563603841
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs1299035553

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151100721_151100724del , CM000667.2:g.151100721_151100724del GRCh38
NC_000005.9:g.150480282_150480285del , CM000667.1:g.150480282_150480285del GRCh37
NC_000005.8:g.150460475_150460478del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*725_*728del MANE Select ENSP00000346550.5:n.*725_*728del
ENST00000522664.5:c.440_443del
NM_001155.4:c.*725_*728del NP_001146.2:n.*725_*728del
NM_001193544.1:c.*725_*728del NP_001180473.1:n.*725_*728del
NM_001363114.1:c.*725_*728del NP_001350043.1:n.*725_*728del
NM_001155.5:c.*725_*728del MANE Select NP_001146.2:n.*725_*728del
NM_001193544.2:c.*725_*728del NP_001180473.1:n.*725_*728del
NM_001363114.2:c.*725_*728del NP_001350043.1:n.*725_*728del