Canonical Allele Identifier: CA1672894476

Gene: ARMT1

Linked Data

• dbSNP Id: rs1781549780
• gnomAD v4: 6-151468286-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468286G>A , CM000668.2:g.151468286G>A	GRCh38
NC_000006.11:g.151789421G>A , CM000668.1:g.151789421G>A	GRCh37
NC_000006.10:g.151831114G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-57G>A MANE Select	ENSP00000356263.3:n.559-57G>A
ENST00000367294.3:c.559-57G>A	ENSP00000356263.3:n.559-57G>A
ENST00000494826.1:c.*282-57G>A	ENSP00000435882.1:n.*282-57G>A
ENST00000545879.5:c.202-57G>A	ENSP00000444121.1:n.202-57G>A
NM_001286562.1:c.202-57G>A	NP_001273491.1:n.202-57G>A
NM_024573.2:c.559-57G>A	NP_078849.1:n.559-57G>A
NM_024573.3:c.559-57G>A MANE Select	NP_078849.1:n.559-57G>A
NM_001286562.2:c.202-57G>A	NP_001273491.1:n.202-57G>A