Canonical Allele Identifier: CA2680797822
Gene: ARMT1 HGNC NCBI

Linked Data

gnomAD v4: 6-151468208-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151468208T>A , CM000668.2:g.151468208T>A GRCh38
NC_000006.11:g.151789343T>A , CM000668.1:g.151789343T>A GRCh37
NC_000006.10:g.151831036T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000367294.4:c.559-135T>A MANE Select ENSP00000356263.3:n.559-135T>A
ENST00000367294.3:c.559-135T>A ENSP00000356263.3:n.559-135T>A
ENST00000494826.1:c.*282-135T>A ENSP00000435882.1:n.*282-135T>A
ENST00000545879.5:c.202-135T>A ENSP00000444121.1:n.202-135T>A
NM_001286562.1:c.202-135T>A NP_001273491.1:n.202-135T>A
NM_024573.2:c.559-135T>A NP_078849.1:n.559-135T>A
NM_024573.3:c.559-135T>A MANE Select NP_078849.1:n.559-135T>A
NM_001286562.2:c.202-135T>A NP_001273491.1:n.202-135T>A
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