Canonical Allele Identifier: CA15707046

Gene: ANO3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.26583784T>C , CM000673.2:g.26583784T>C	GRCh38
NC_000011.9:g.26605331T>C , CM000673.1:g.26605331T>C	GRCh37
NC_000011.8:g.26561907T>C	NCBI36
NG_042856.1:g.399662T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256737.8:c.1448-14581T>C MANE Select	ENSP00000256737.3:n.1448-14581T>C
ENST00000672621.1:c.1631-14581T>C	ENSP00000500506.1:n.1631-14581T>C
ENST00000256737.7:c.1448-14581T>C	ENSP00000256737.3:n.1448-14581T>C
ENST00000525139.5:c.1400-14581T>C	ENSP00000432576.1:n.1400-14581T>C
ENST00000531568.1:c.1010-14581T>C	ENSP00000432394.1:n.1010-14581T>C
NM_001313726.1:c.1631-14581T>C	NP_001300655.1:n.1631-14581T>C
NM_001313727.1:c.1010-14581T>C	NP_001300656.1:n.1010-14581T>C
NM_031418.2:c.1448-14581T>C	NP_113606.2:n.1448-14581T>C
NM_031418.3:c.1448-14581T>C	NP_113606.2:n.1448-14581T>C
XM_011520282.1:c.49+10535T>C	XP_011518584.1:n.49+10535T>C
XM_011520282.3:c.49+10535T>C	XP_011518584.1:n.49+10535T>C
XM_017018118.2:c.1010-14581T>C	XP_016873607.1:n.1010-14581T>C
XM_017018119.2:c.719-14581T>C	XP_016873608.1:n.719-14581T>C
NM_031418.4:c.1448-14581T>C MANE Select	NP_113606.2:n.1448-14581T>C
NM_001313726.2:c.1631-14581T>C	NP_001300655.1:n.1631-14581T>C
NM_001313727.2:c.1010-14581T>C	NP_001300656.1:n.1010-14581T>C