Canonical Allele Identifier: CA2669788289
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4862549-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862549A>T , CM000666.2:g.4862549A>T GRCh38
NC_000004.11:g.4864276A>T , CM000666.1:g.4864276A>T GRCh37
NC_000004.10:g.4915177A>T NCBI36
NG_008121.1:g.7885A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-152A>T MANE Select ENSP00000372170.4:n.470-152A>T
ENST00000382723.4:c.470-152A>T ENSP00000372170.4:n.470-152A>T
ENST00000468421.1:n.122A>T
NM_002448.3:c.470-152A>T MANE Select NP_002439.2:n.470-152A>T
Search 100 bp 5'
Search 100 bp 3'