Canonical Allele Identifier: CA1591241101
Gene: ANXA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151101006T= , CM000667.2:g.151101006T= GRCh38
NC_000005.9:g.150480567T= , CM000667.1:g.150480567T= GRCh37
NC_000005.8:g.150460760T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*442A= MANE Select ENSP00000346550.5:n.*442A=
ENST00000522664.5:c.201-44A=
NM_001155.4:c.*442A= NP_001146.2:n.*442A=
NM_001193544.1:c.*442A= NP_001180473.1:n.*442A=
NM_001363114.1:c.*442A= NP_001350043.1:n.*442A=
NM_001155.5:c.*442A= MANE Select NP_001146.2:n.*442A=
NM_001193544.2:c.*442A= NP_001180473.1:n.*442A=
NM_001363114.2:c.*442A= NP_001350043.1:n.*442A=