Canonical Allele Identifier: CA14447916

Gene: ASIC2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.33066684C>T , CM000679.2:g.33066684C>T	GRCh38
NC_000017.10:g.31393702C>T , CM000679.1:g.31393702C>T	GRCh37
NC_000017.9:g.28417815C>T	NCBI36
NG_029763.1:g.1095124G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225823.7:c.987+22179G>A MANE Select	ENSP00000225823.2:n.987+22179G>A
ENST00000225823.6:c.987+22179G>A	ENSP00000225823.2:n.987+22179G>A
ENST00000359872.6:c.834+22179G>A	ENSP00000352934.6:n.834+22179G>A
ENST00000448983.1:n.392+22179G>A
NM_001094.4:c.834+22179G>A	NP_001085.2:n.834+22179G>A
NM_183377.1:c.987+22179G>A	NP_899233.1:n.987+22179G>A
NM_001094.5:c.834+22179G>A	NP_001085.2:n.834+22179G>A
NM_183377.2:c.987+22179G>A MANE Select	NP_899233.1:n.987+22179G>A