Canonical Allele Identifier: CA379935636

Gene: ANO3 MUC15

Linked Data

• COSMIC: COSM6445647 ; COSM6445648
• MyVariant Identifiers: chr11:g.26586710A>G (hg19) ; chr11:g.26565163A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.26565163A>G , CM000673.2:g.26565163A>G	GRCh38
NC_000011.9:g.26586710A>G , CM000673.1:g.26586710A>G	GRCh37
NC_000011.8:g.26543286A>G	NCBI36
NG_042856.1:g.381041A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000256737.8:c.1447+5384A>G (ANO3) MANE Select	ENSP00000256737.3:n.1447+5384A>G
ENST00000529533.6:c.775+2T>C (MUC15) MANE Select	ENSP00000431983.1:n.775+2T>C
ENST00000672621.1:c.1630+5384A>G (ANO3)	ENSP00000500506.1:n.1630+5384A>G
ENST00000256737.7:c.1447+5384A>G (ANO3)	ENSP00000256737.3:n.1447+5384A>G
ENST00000281268.12:c.775+2T>C (MUC15)	ENSP00000281268.8:n.775+2T>C
ENST00000436318.6:c.775+2T>C (MUC15)	ENSP00000416753.2:n.775+2T>C
ENST00000455601.6:c.694+2T>C (MUC15)	ENSP00000397339.2:n.694+2T>C
ENST00000525139.5:c.1399+5384A>G (ANO3)	ENSP00000432576.1:n.1399+5384A>G
ENST00000527569.1:c.775+2T>C (MUC15)	ENSP00000431945.1:n.775+2T>C
ENST00000529533.5:c.775+2T>C (MUC15)	ENSP00000431983.1:n.775+2T>C
ENST00000531568.1:c.1009+5384A>G (ANO3)	ENSP00000432394.1:n.1009+5384A>G
NM_001135091.1:c.775+2T>C (MUC15)	NP_001128563.1:n.775+2T>C
NM_001135092.1:c.775+2T>C (MUC15)	NP_001128564.1:n.775+2T>C
NM_001313726.1:c.1630+5384A>G (ANO3)	NP_001300655.1:n.1630+5384A>G
NM_001313727.1:c.1009+5384A>G (ANO3)	NP_001300656.1:n.1009+5384A>G
NM_031418.2:c.1447+5384A>G (ANO3)	NP_113606.2:n.1447+5384A>G
NM_031418.3:c.1447+5384A>G (ANO3)	NP_113606.2:n.1447+5384A>G
NM_145650.3:c.694+2T>C (MUC15)	NP_663625.2:n.694+2T>C
XM_011519908.1:c.1042+2T>C (MUC15)	XP_011518210.1:n.1042+2T>C
XM_011519909.1:c.1042+2T>C (MUC15)	XP_011518211.1:n.1042+2T>C
XM_017018118.2:c.1009+5384A>G (ANO3)	XP_016873607.1:n.1009+5384A>G
XM_017018119.2:c.718+5384A>G (ANO3)	XP_016873608.1:n.718+5384A>G
NM_001135091.2:c.775+2T>C (MUC15) MANE Select	NP_001128563.1:n.775+2T>C
NM_031418.4:c.1447+5384A>G (ANO3) MANE Select	NP_113606.2:n.1447+5384A>G
NM_001135092.2:c.775+2T>C (MUC15)	NP_001128564.1:n.775+2T>C
NM_145650.4:c.694+2T>C (MUC15)	NP_663625.2:n.694+2T>C
NM_001313726.2:c.1630+5384A>G (ANO3)	NP_001300655.1:n.1630+5384A>G
NM_001313727.2:c.1009+5384A>G (ANO3)	NP_001300656.1:n.1009+5384A>G