Canonical Allele Identifier: CA1591241160
Gene: ANXA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151101114C= , CM000667.2:g.151101114C= GRCh38
NC_000005.9:g.150480675C= , CM000667.1:g.150480675C= GRCh37
NC_000005.8:g.150460868C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*334G= MANE Select ENSP00000346550.5:n.*334G=
ENST00000354546.9:c.*334G= ENSP00000346550.5:n.*334G=
ENST00000377751.9:c.*334G= ENSP00000366980.5:n.*334G=
ENST00000522664.5:c.201-152G=
ENST00000523714.5:c.*334G= ENSP00000430517.1:n.*334G=
NM_001155.4:c.*334G= NP_001146.2:n.*334G=
NM_001193544.1:c.*334G= NP_001180473.1:n.*334G=
XM_005268432.3:c.*334G= XP_005268489.1:n.*334G=
NM_001363114.1:c.*334G= NP_001350043.1:n.*334G=
NM_001155.5:c.*334G= MANE Select NP_001146.2:n.*334G=
NM_001193544.2:c.*334G= NP_001180473.1:n.*334G=
NM_001363114.2:c.*334G= NP_001350043.1:n.*334G=