Canonical Allele Identifier: CA2768909833
Gene: ANXA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151101103C>T , CM000667.2:g.151101103C>T GRCh38
NC_000005.9:g.150480664C>T , CM000667.1:g.150480664C>T GRCh37
NC_000005.8:g.150460857C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*345G>A MANE Select ENSP00000346550.5:n.*345G>A
ENST00000522664.5:c.201-141G>A
NM_001155.4:c.*345G>A NP_001146.2:n.*345G>A
NM_001193544.1:c.*345G>A NP_001180473.1:n.*345G>A
XM_005268432.3:c.*345G>A XP_005268489.1:n.*345G>A
NM_001363114.1:c.*345G>A NP_001350043.1:n.*345G>A
NM_001155.5:c.*345G>A MANE Select NP_001146.2:n.*345G>A
NM_001193544.2:c.*345G>A NP_001180473.1:n.*345G>A
NM_001363114.2:c.*345G>A NP_001350043.1:n.*345G>A