Canonical Allele Identifier: CA2680797847

Gene: ARMT1

Linked Data

• gnomAD v4: 6-151468214-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468214T>G , CM000668.2:g.151468214T>G	GRCh38
NC_000006.11:g.151789349T>G , CM000668.1:g.151789349T>G	GRCh37
NC_000006.10:g.151831042T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-129T>G MANE Select	ENSP00000356263.3:n.559-129T>G
ENST00000367294.3:c.559-129T>G	ENSP00000356263.3:n.559-129T>G
ENST00000494826.1:c.*282-129T>G	ENSP00000435882.1:n.*282-129T>G
ENST00000545879.5:c.202-129T>G	ENSP00000444121.1:n.202-129T>G
NM_001286562.1:c.202-129T>G	NP_001273491.1:n.202-129T>G
NM_024573.2:c.559-129T>G	NP_078849.1:n.559-129T>G
NM_024573.3:c.559-129T>G MANE Select	NP_078849.1:n.559-129T>G
NM_001286562.2:c.202-129T>G	NP_001273491.1:n.202-129T>G