Canonical Allele Identifier: CA6525350
Gene: ANO6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45401794G>T , CM000674.2:g.45401794G>T GRCh38
NC_000012.11:g.45795577G>T , CM000674.1:g.45795577G>T GRCh37
NC_000012.10:g.44081844G>T NCBI36
NG_028220.1:g.190808G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320560.13:c.1387-1G>T MANE Select ENSP00000320087.8:n.1387-1G>T
ENST00000679426.1:c.1354-1G>T ENSP00000506600.1:n.1354-1G>T
ENST00000679761.1:c.1387-1G>T ENSP00000505361.1:n.1387-1G>T
ENST00000680201.1:c.1387-1G>T ENSP00000506222.1:n.1387-1G>T
ENST00000680371.1:c.1387-1G>T ENSP00000506392.1:n.1387-1G>T
ENST00000680498.1:c.970-1G>T ENSP00000506613.1:n.970-1G>T
ENST00000681156.1:c.1387-1G>T ENSP00000506069.1:n.1387-1G>T
ENST00000681817.1:c.970-1G>T ENSP00000506683.1:n.970-1G>T
ENST00000320560.12:c.1387-1G>T ENSP00000320087.8:n.1387-1G>T
ENST00000423947.7:c.1450-1G>T ENSP00000409126.3:n.1450-1G>T
ENST00000425752.6:c.1387-1G>T ENSP00000391417.2:n.1387-1G>T
ENST00000426898.2:n.1803-1G>T
ENST00000441606.2:c.1333-1G>T ENSP00000413137.2:n.1333-1G>T
NM_001025356.2:c.1387-1G>T NP_001020527.2:n.1387-1G>T
NM_001142678.1:c.1333-1G>T NP_001136150.1:n.1333-1G>T
NM_001142679.1:c.1387-1G>T NP_001136151.1:n.1387-1G>T
NM_001204803.1:c.1450-1G>T NP_001191732.1:n.1450-1G>T
XM_005268706.3:c.1354-1G>T XP_005268763.1:n.1354-1G>T
XM_005268707.2:c.1288-1G>T XP_005268764.1:n.1288-1G>T
XM_011538024.1:c.1450-1G>T XP_011536326.1:n.1450-1G>T
XR_944886.1:n.1352-3570C>A
XR_944888.1:n.1352-3570C>A
XM_005268706.5:c.1354-1G>T XP_005268763.1:n.1354-1G>T
XM_005268707.4:c.1288-1G>T XP_005268764.1:n.1288-1G>T
XR_001749096.1:n.1353-3570C>A
XR_944886.2:n.1353-3570C>A
NM_001025356.3:c.1387-1G>T MANE Select NP_001020527.2:n.1387-1G>T
NM_001142678.2:c.1333-1G>T NP_001136150.1:n.1333-1G>T
NM_001142679.2:c.1387-1G>T NP_001136151.1:n.1387-1G>T
NM_001204803.2:c.1450-1G>T NP_001191732.1:n.1450-1G>T