Canonical Allele Identifier: CA2676572779
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174725091-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174725097del , CM000667.2:g.174725097del GRCh38
NC_000005.9:g.174152100del , CM000667.1:g.174152100del GRCh37
NC_000005.8:g.174084706del NCBI36
NG_008124.1:g.5526del

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.379+59del MANE Select ENSP00000239243.5:n.379+59del
ENST00000239243.6:c.379+59del ENSP00000239243.5:n.379+59del
ENST00000507785.2:c.*3+30del ENSP00000427425.1:n.*3+30del
NM_002449.4:c.379+59del NP_002440.2:n.379+59del
NM_001363626.1:c.*3+30del NP_001350555.1:n.*3+30del
NM_002449.5:c.379+59del MANE Select NP_002440.2:n.379+59del
NM_001363626.2:c.*3+30del NP_001350555.1:n.*3+30del
Search 100 bp 5'
Search 100 bp 3'