Canonical Allele Identifier: CA947192526
Gene: ANO6 HGNC NCBI

Linked Data

dbSNP Id: rs1942845617

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.45403337A>G , CM000674.2:g.45403337A>G GRCh38
NC_000012.11:g.45797120A>G , CM000674.1:g.45797120A>G GRCh37
NC_000012.10:g.44083387A>G NCBI36
NG_028220.1:g.192351A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320560.13:c.1782+96A>G MANE Select ENSP00000320087.8:n.1782+96A>G
ENST00000679426.1:c.1749+96A>G ENSP00000506600.1:n.1749+96A>G
ENST00000679761.1:c.1782+96A>G ENSP00000505361.1:n.1782+96A>G
ENST00000680201.1:c.1782+96A>G ENSP00000506222.1:n.1782+96A>G
ENST00000680371.1:c.1782+96A>G ENSP00000506392.1:n.1782+96A>G
ENST00000680498.1:c.1365+96A>G ENSP00000506613.1:n.1365+96A>G
ENST00000681156.1:c.1782+96A>G ENSP00000506069.1:n.1782+96A>G
ENST00000681817.1:c.1365+96A>G ENSP00000506683.1:n.1365+96A>G
ENST00000320560.12:c.1782+96A>G ENSP00000320087.8:n.1782+96A>G
ENST00000423947.7:c.1845+96A>G ENSP00000409126.3:n.1845+96A>G
ENST00000425752.6:c.1782+96A>G ENSP00000391417.2:n.1782+96A>G
ENST00000426898.2:n.2198+96A>G
ENST00000441606.2:c.1728+96A>G ENSP00000413137.2:n.1728+96A>G
NM_001025356.2:c.1782+96A>G NP_001020527.2:n.1782+96A>G
NM_001142678.1:c.1728+96A>G NP_001136150.1:n.1728+96A>G
NM_001142679.1:c.1782+96A>G NP_001136151.1:n.1782+96A>G
NM_001204803.1:c.1845+96A>G NP_001191732.1:n.1845+96A>G
XM_005268706.3:c.1749+96A>G XP_005268763.1:n.1749+96A>G
XM_005268707.2:c.1683+96A>G XP_005268764.1:n.1683+96A>G
XM_011538024.1:c.1845+96A>G XP_011536326.1:n.1845+96A>G
XR_944886.1:n.1352-5113T>C
XR_944888.1:n.1352-5113T>C
XM_005268706.5:c.1749+96A>G XP_005268763.1:n.1749+96A>G
XM_005268707.4:c.1683+96A>G XP_005268764.1:n.1683+96A>G
XR_001749096.1:n.1353-5113T>C
XR_944886.2:n.1353-5113T>C
NM_001025356.3:c.1782+96A>G MANE Select NP_001020527.2:n.1782+96A>G
NM_001142678.2:c.1728+96A>G NP_001136150.1:n.1728+96A>G
NM_001142679.2:c.1782+96A>G NP_001136151.1:n.1782+96A>G
NM_001204803.2:c.1845+96A>G NP_001191732.1:n.1845+96A>G