Canonical Allele Identifier: CA820835095

Gene: ARMT1

Linked Data

• dbSNP Id: rs1371425549
• gnomAD v3: 6-151468155-CTTG-C
• gnomAD v4: 6-151468155-CTTG-C
• MyVariant Identifiers: chr6:g.151789291_151789293del (hg19) ; chr6:g.151468156_151468158del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468158_151468160del , CM000668.2:g.151468158_151468160del	GRCh38
NC_000006.11:g.151789293_151789295del , CM000668.1:g.151789293_151789295del	GRCh37
NC_000006.10:g.151830986_151830988del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-185_559-183del MANE Select	ENSP00000356263.3:n.559-185_559-183del
ENST00000367294.3:c.559-185_559-183del	ENSP00000356263.3:n.559-185_559-183del
ENST00000494826.1:c.*282-185_*282-183del	ENSP00000435882.1:n.*282-185_*282-183del
ENST00000545879.5:c.202-185_202-183del	ENSP00000444121.1:n.202-185_202-183del
NM_001286562.1:c.202-185_202-183del	NP_001273491.1:n.202-185_202-183del
NM_024573.2:c.559-185_559-183del	NP_078849.1:n.559-185_559-183del
NM_024573.3:c.559-185_559-183del MANE Select	NP_078849.1:n.559-185_559-183del
NM_001286562.2:c.202-185_202-183del	NP_001273491.1:n.202-185_202-183del