Canonical Allele Identifier: CA2680797796

Gene: ARMT1

Linked Data

• gnomAD v4: 6-151468200-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468200A>C , CM000668.2:g.151468200A>C	GRCh38
NC_000006.11:g.151789335A>C , CM000668.1:g.151789335A>C	GRCh37
NC_000006.10:g.151831028A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-143A>C MANE Select	ENSP00000356263.3:n.559-143A>C
ENST00000367294.3:c.559-143A>C	ENSP00000356263.3:n.559-143A>C
ENST00000494826.1:c.*282-143A>C	ENSP00000435882.1:n.*282-143A>C
ENST00000545879.5:c.202-143A>C	ENSP00000444121.1:n.202-143A>C
NM_001286562.1:c.202-143A>C	NP_001273491.1:n.202-143A>C
NM_024573.2:c.559-143A>C	NP_078849.1:n.559-143A>C
NM_024573.3:c.559-143A>C MANE Select	NP_078849.1:n.559-143A>C
NM_001286562.2:c.202-143A>C	NP_001273491.1:n.202-143A>C