Canonical Allele Identifier: CA13569214

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.26568579G>A , CM000673.2:g.26568579G>A GRCh38
NC_000011.9:g.26590126G>A , CM000673.1:g.26590126G>A GRCh37
NC_000011.8:g.26546702G>A NCBI36
NG_042856.1:g.384457G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256737.8:c.1447+8800G>A (ANO3) MANE Select ENSP00000256737.3:n.1447+8800G>A
ENST00000529533.6:c.-45-1440C>T (MUC15) MANE Select ENSP00000431983.1:n.-45-1440C>T
ENST00000648230.1:c.-46+895C>T (MUC15) ENSP00000498053.1:n.-46+895C>T
ENST00000672621.1:c.1630+8800G>A (ANO3) ENSP00000500506.1:n.1630+8800G>A
ENST00000256737.7:c.1447+8800G>A (ANO3) ENSP00000256737.3:n.1447+8800G>A
ENST00000455601.6:c.-38-2683C>T (MUC15) ENSP00000397339.2:n.-38-2683C>T
ENST00000525139.5:c.1399+8800G>A (ANO3) ENSP00000432576.1:n.1399+8800G>A
ENST00000527569.1:c.-45-1440C>T (MUC15) ENSP00000431945.1:n.-45-1440C>T
ENST00000529533.5:c.-45-1440C>T (MUC15) ENSP00000431983.1:n.-45-1440C>T
ENST00000531568.1:c.1009+8800G>A (ANO3) ENSP00000432394.1:n.1009+8800G>A
NM_001135091.1:c.-45-1440C>T (MUC15) NP_001128563.1:n.-45-1440C>T
NM_001135092.1:c.-45-1440C>T (MUC15) NP_001128564.1:n.-45-1440C>T
NM_001313726.1:c.1630+8800G>A (ANO3) NP_001300655.1:n.1630+8800G>A
NM_001313727.1:c.1009+8800G>A (ANO3) NP_001300656.1:n.1009+8800G>A
NM_031418.2:c.1447+8800G>A (ANO3) NP_113606.2:n.1447+8800G>A
NM_031418.3:c.1447+8800G>A (ANO3) NP_113606.2:n.1447+8800G>A
NM_145650.3:c.-38-2683C>T (MUC15) NP_663625.2:n.-38-2683C>T
XM_011519908.1:c.223-1440C>T (MUC15) XP_011518210.1:n.223-1440C>T
XM_011519909.1:c.223-1440C>T (MUC15) XP_011518211.1:n.223-1440C>T
XM_017018118.2:c.1009+8800G>A (ANO3) XP_016873607.1:n.1009+8800G>A
XM_017018119.2:c.718+8800G>A (ANO3) XP_016873608.1:n.718+8800G>A
NM_001135091.2:c.-45-1440C>T (MUC15) MANE Select NP_001128563.1:n.-45-1440C>T
NM_031418.4:c.1447+8800G>A (ANO3) MANE Select NP_113606.2:n.1447+8800G>A
NM_001135092.2:c.-45-1440C>T (MUC15) NP_001128564.1:n.-45-1440C>T
NM_145650.4:c.-38-2683C>T (MUC15) NP_663625.2:n.-38-2683C>T
NM_001313726.2:c.1630+8800G>A (ANO3) NP_001300655.1:n.1630+8800G>A
NM_001313727.2:c.1009+8800G>A (ANO3) NP_001300656.1:n.1009+8800G>A