Canonical Allele Identifier: CA1591257543
Gene: ANXA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151137464C= , CM000667.2:g.151137464C= GRCh38
NC_000005.9:g.150517025C= , CM000667.1:g.150517025C= GRCh37
NC_000005.8:g.150497218C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000700367.1:c.319-143G= ENSP00000514965.1:n.319-143G=
ENST00000354546.10:c.319-143G= MANE Select ENSP00000346550.5:n.319-143G=
ENST00000354546.9:c.319-143G= ENSP00000346550.5:n.319-143G=
ENST00000377751.9:c.204+1889G= ENSP00000366980.5:n.204+1889G=
ENST00000517486.5:c.318+1214G= ENSP00000428916.1:n.318+1214G=
ENST00000517677.5:c.319-143G= ENSP00000430826.1:n.319-143G=
ENST00000517757.5:c.223-143G= ENSP00000430572.1:n.223-143G=
ENST00000519644.6:c.262+1270G= ENSP00000430663.2:n.262+1270G=
ENST00000520378.1:n.1011-143G=
ENST00000521512.5:c.224+1308G= ENSP00000430420.1:n.224+1308G=
ENST00000521749.5:c.223-143G= ENSP00000430429.1:n.223-143G=
ENST00000523164.1:c.319-143G= ENSP00000431078.1:n.319-143G=
ENST00000523714.5:c.223-143G= ENSP00000430517.1:n.223-143G=
NM_001155.4:c.319-143G= NP_001146.2:n.319-143G=
NM_001193544.1:c.223-143G= NP_001180473.1:n.223-143G=
XM_005268432.3:c.319-143G= XP_005268489.1:n.319-143G=
NM_001363114.1:c.319-143G= NP_001350043.1:n.319-143G=
NM_001155.5:c.319-143G= MANE Select NP_001146.2:n.319-143G=
NM_001193544.2:c.223-143G= NP_001180473.1:n.223-143G=
NM_001363114.2:c.319-143G= NP_001350043.1:n.319-143G=