Canonical Allele Identifier: CA2676572669
Gene: MSX2 HGNC NCBI

Linked Data

gnomAD v4: 5-174724592-AGTTTGAGTCGCCGCTGCCG-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724594_174724612del , CM000667.2:g.174724594_174724612del GRCh38
NC_000005.9:g.174151597_174151615del , CM000667.1:g.174151597_174151615del GRCh37
NC_000005.8:g.174084203_174084221del NCBI36
NG_008124.1:g.5023_5041del

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.-66_-48del MANE Select ENSP00000239243.5:n.-66_-48del
ENST00000239243.6:c.-66_-48del ENSP00000239243.5:n.-66_-48del
NM_002449.4:c.-66_-48del NP_002440.2:n.-66_-48del
NM_001363626.1:c.-66_-48del NP_001350555.1:n.-66_-48del
NM_002449.5:c.-66_-48del MANE Select NP_002440.2:n.-66_-48del
NM_001363626.2:c.-66_-48del NP_001350555.1:n.-66_-48del
Search 100 bp 5'
Search 100 bp 3'