Canonical Allele Identifier: CA1602346612
Gene: MSX2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174725002_174725003delinsTG , CM000667.2:g.174725002_174725003delinsTG GRCh38
NC_000005.9:g.174152005_174152006delinsTG , CM000667.1:g.174152005_174152006delinsTG GRCh37
NC_000005.8:g.174084611_174084612delinsTG NCBI36
NG_008124.1:g.5431_5432delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.343_344delinsTG MANE Select ENSP00000239243.5:p.Trp115=
ENST00000239243.6:c.343_344delinsTG ENSP00000239243.5:p.Trp115=
ENST00000507785.2:c.343_344delinsTG ENSP00000427425.1:p.Trp115=
NM_002449.4:c.343_344delinsTG NP_002440.2:p.Trp115=
NM_001363626.1:c.343_344delinsTG NP_001350555.1:p.Trp115=
NM_002449.5:c.343_344delinsTG MANE Select NP_002440.2:p.Trp115=
NM_001363626.2:c.343_344delinsTG NP_001350555.1:p.Trp115=
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