Canonical Allele Identifier: CA1435013809
Gene: MSX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863115_4863116delinsTG , CM000666.2:g.4863115_4863116delinsTG GRCh38
NC_000004.11:g.4864842_4864843delinsTG , CM000666.1:g.4864842_4864843delinsTG GRCh37
NC_000004.10:g.4915743_4915744delinsTG NCBI36
NG_008121.1:g.8451_8452delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.884_885delinsTG MANE Select ENSP00000372170.4:p.Val295=
ENST00000382723.4:c.884_885delinsTG ENSP00000372170.4:p.Val295=
NM_002448.3:c.884_885delinsTG MANE Select NP_002439.2:p.Val295=
Search 100 bp 5'
Search 100 bp 3'