Canonical Allele Identifier: CA571124487

Gene: ARMT1

Linked Data

• gnomAD v2: 6-151789337-A-G
• gnomAD v4: 6-151468202-A-G
• MyVariant Identifiers: chr6:g.151789337A>G (hg19) ; chr6:g.151468202A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468202A>G , CM000668.2:g.151468202A>G	GRCh38
NC_000006.11:g.151789337A>G , CM000668.1:g.151789337A>G	GRCh37
NC_000006.10:g.151831030A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-141A>G MANE Select	ENSP00000356263.3:n.559-141A>G
ENST00000367294.3:c.559-141A>G	ENSP00000356263.3:n.559-141A>G
ENST00000494826.1:c.*282-141A>G	ENSP00000435882.1:n.*282-141A>G
ENST00000545879.5:c.202-141A>G	ENSP00000444121.1:n.202-141A>G
NM_001286562.1:c.202-141A>G	NP_001273491.1:n.202-141A>G
NM_024573.2:c.559-141A>G	NP_078849.1:n.559-141A>G
NM_024573.3:c.559-141A>G MANE Select	NP_078849.1:n.559-141A>G
NM_001286562.2:c.202-141A>G	NP_001273491.1:n.202-141A>G