Canonical Allele Identifier: CA1591241156
Gene: ANXA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151101109A= , CM000667.2:g.151101109A= GRCh38
NC_000005.9:g.150480670A= , CM000667.1:g.150480670A= GRCh37
NC_000005.8:g.150460863A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*339T= MANE Select ENSP00000346550.5:n.*339T=
ENST00000354546.9:c.*339T= ENSP00000346550.5:n.*339T=
ENST00000377751.9:c.*339T= ENSP00000366980.5:n.*339T=
ENST00000522664.5:c.201-147T=
ENST00000523714.5:c.*339T= ENSP00000430517.1:n.*339T=
NM_001155.4:c.*339T= NP_001146.2:n.*339T=
NM_001193544.1:c.*339T= NP_001180473.1:n.*339T=
XM_005268432.3:c.*339T= XP_005268489.1:n.*339T=
NM_001363114.1:c.*339T= NP_001350043.1:n.*339T=
NM_001155.5:c.*339T= MANE Select NP_001146.2:n.*339T=
NM_001193544.2:c.*339T= NP_001180473.1:n.*339T=
NM_001363114.2:c.*339T= NP_001350043.1:n.*339T=