Canonical Allele Identifier: CA2676572689
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174724610-CG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724613del , CM000667.2:g.174724613del GRCh38
NC_000005.9:g.174151616del , CM000667.1:g.174151616del GRCh37
NC_000005.8:g.174084222del NCBI36
NG_008124.1:g.5042del

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-47del MANE Select ENSP00000239243.5:n.-47del
ENST00000239243.6:c.-47del ENSP00000239243.5:n.-47del
ENST00000507785.2:c.-47del ENSP00000427425.1:n.-47del
NM_002449.4:c.-47del NP_002440.2:n.-47del
NM_001363626.1:c.-47del NP_001350555.1:n.-47del
NM_002449.5:c.-47del MANE Select NP_002440.2:n.-47del
NM_001363626.2:c.-47del NP_001350555.1:n.-47del
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