Canonical Allele Identifier: CA1591252343
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs1765300173

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151125828C>G , CM000667.2:g.151125828C>G GRCh38
NC_000005.9:g.150505389C>G , CM000667.1:g.150505389C>G GRCh37
NC_000005.8:g.150485582C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000700367.1:c.1056+574G>C ENSP00000514965.1:n.1056+574G>C
ENST00000354546.10:c.1056+574G>C MANE Select ENSP00000346550.5:n.1056+574G>C
ENST00000354546.9:c.1056+574G>C ENSP00000346550.5:n.1056+574G>C
ENST00000377751.9:c.205-3568G>C ENSP00000366980.5:n.205-3568G>C
ENST00000517486.5:c.318+12850G>C ENSP00000428916.1:n.318+12850G>C
ENST00000519644.6:c.*19+574G>C ENSP00000430663.2:n.*19+574G>C
ENST00000520054.1:n.270+574G>C
ENST00000521512.5:c.435+574G>C ENSP00000430420.1:n.435+574G>C
ENST00000523714.5:c.960+574G>C ENSP00000430517.1:n.960+574G>C
NM_001155.4:c.1056+574G>C NP_001146.2:n.1056+574G>C
NM_001193544.1:c.960+574G>C NP_001180473.1:n.960+574G>C
XM_005268432.3:c.1056+574G>C XP_005268489.1:n.1056+574G>C
NM_001363114.1:c.1056+574G>C NP_001350043.1:n.1056+574G>C
NM_001155.5:c.1056+574G>C MANE Select NP_001146.2:n.1056+574G>C
NM_001193544.2:c.960+574G>C NP_001180473.1:n.960+574G>C
NM_001363114.2:c.1056+574G>C NP_001350043.1:n.1056+574G>C