Canonical Allele Identifier: CA2676572662
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174724586-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724592del , CM000667.2:g.174724592del GRCh38
NC_000005.9:g.174151595del , CM000667.1:g.174151595del GRCh37
NC_000005.8:g.174084201del NCBI36
NG_008124.1:g.5021del

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-68del MANE Select ENSP00000239243.5:n.-68del
ENST00000239243.6:c.-68del ENSP00000239243.5:n.-68del
NM_002449.4:c.-68del NP_002440.2:n.-68del
NM_001363626.1:c.-68del NP_001350555.1:n.-68del
NM_002449.5:c.-68del MANE Select NP_002440.2:n.-68del
NM_001363626.2:c.-68del NP_001350555.1:n.-68del
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