Canonical Allele Identifier: CA2680797829

Gene: ARMT1

Linked Data

• gnomAD v4: 6-151468210-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151468210G>C , CM000668.2:g.151468210G>C	GRCh38
NC_000006.11:g.151789345G>C , CM000668.1:g.151789345G>C	GRCh37
NC_000006.10:g.151831038G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367294.4:c.559-133G>C MANE Select	ENSP00000356263.3:n.559-133G>C
ENST00000367294.3:c.559-133G>C	ENSP00000356263.3:n.559-133G>C
ENST00000494826.1:c.*282-133G>C	ENSP00000435882.1:n.*282-133G>C
ENST00000545879.5:c.202-133G>C	ENSP00000444121.1:n.202-133G>C
NM_001286562.1:c.202-133G>C	NP_001273491.1:n.202-133G>C
NM_024573.2:c.559-133G>C	NP_078849.1:n.559-133G>C
NM_024573.3:c.559-133G>C MANE Select	NP_078849.1:n.559-133G>C
NM_001286562.2:c.202-133G>C	NP_001273491.1:n.202-133G>C