Canonical Allele Identifier: CA2676049906
Gene: ANXA6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151101120T>A , CM000667.2:g.151101120T>A GRCh38
NC_000005.9:g.150480681T>A , CM000667.1:g.150480681T>A GRCh37
NC_000005.8:g.150460874T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*328A>T MANE Select ENSP00000346550.5:n.*328A>T
ENST00000354546.9:c.*328A>T ENSP00000346550.5:n.*328A>T
ENST00000377751.9:c.*328A>T ENSP00000366980.5:n.*328A>T
ENST00000522664.5:c.201-158A>T
ENST00000523714.5:c.*328A>T ENSP00000430517.1:n.*328A>T
NM_001155.4:c.*328A>T NP_001146.2:n.*328A>T
NM_001193544.1:c.*328A>T NP_001180473.1:n.*328A>T
XM_005268432.3:c.*328A>T XP_005268489.1:n.*328A>T
NM_001363114.1:c.*328A>T NP_001350043.1:n.*328A>T
NM_001155.5:c.*328A>T MANE Select NP_001146.2:n.*328A>T
NM_001193544.2:c.*328A>T NP_001180473.1:n.*328A>T
NM_001363114.2:c.*328A>T NP_001350043.1:n.*328A>T