Canonical Allele Identifier: CA2680797788

Gene: ARMT1

Linked Data

• gnomAD v4: 6-151468197-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468197T>C , CM000668.2:g.151468197T>C	GRCh38
NC_000006.11:g.151789332T>C , CM000668.1:g.151789332T>C	GRCh37
NC_000006.10:g.151831025T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-146T>C MANE Select	ENSP00000356263.3:n.559-146T>C
ENST00000367294.3:c.559-146T>C	ENSP00000356263.3:n.559-146T>C
ENST00000494826.1:c.*282-146T>C	ENSP00000435882.1:n.*282-146T>C
ENST00000545879.5:c.202-146T>C	ENSP00000444121.1:n.202-146T>C
NM_001286562.1:c.202-146T>C	NP_001273491.1:n.202-146T>C
NM_024573.2:c.559-146T>C	NP_078849.1:n.559-146T>C
NM_024573.3:c.559-146T>C MANE Select	NP_078849.1:n.559-146T>C
NM_001286562.2:c.202-146T>C	NP_001273491.1:n.202-146T>C