Canonical Allele Identifier: CA2669788635
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4863207-C-CT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863207_4863208insT , CM000666.2:g.4863207_4863208insT GRCh38
NC_000004.11:g.4864934_4864935insT , CM000666.1:g.4864934_4864935insT GRCh37
NC_000004.10:g.4915835_4915836insT NCBI36
NG_008121.1:g.8543_8544insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*64_*65insT MANE Select ENSP00000372170.4:n.*64_*65insT
ENST00000382723.4:c.*64_*65insT ENSP00000372170.4:n.*64_*65insT
NM_002448.3:c.*64_*65insT MANE Select NP_002439.2:n.*64_*65insT
Search 100 bp 5'
Search 100 bp 3'