Canonical Allele Identifier: CA2546818606

Gene: ARMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468160_151468167del , CM000668.2:g.151468160_151468167del	GRCh38
NC_000006.11:g.151789295_151789302del , CM000668.1:g.151789295_151789302del	GRCh37
NC_000006.10:g.151830988_151830995del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-183_559-176del MANE Select	ENSP00000356263.3:n.559-183_559-176del
ENST00000367294.3:c.559-183_559-176del	ENSP00000356263.3:n.559-183_559-176del
ENST00000494826.1:c.*282-183_*282-176del	ENSP00000435882.1:n.*282-183_*282-176del
ENST00000545879.5:c.202-183_202-176del	ENSP00000444121.1:n.202-183_202-176del
NM_001286562.1:c.202-183_202-176del	NP_001273491.1:n.202-183_202-176del
NM_024573.2:c.559-183_559-176del	NP_078849.1:n.559-183_559-176del
NM_024573.3:c.559-183_559-176del MANE Select	NP_078849.1:n.559-183_559-176del
NM_001286562.2:c.202-183_202-176del	NP_001273491.1:n.202-183_202-176del