Canonical Allele Identifier: CA2950777
Community Standard Title: NM_152291.3(MUC7):c.710_778del (p.Ala237_Ala259del)
Gene: MUC7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70481454_70481522del , CM000666.2:g.70481454_70481522del GRCh38
NC_000004.11:g.71347171_71347239del , CM000666.1:g.71347171_71347239del GRCh37
NC_000004.10:g.71381760_71381828del NCBI36
NG_012348.1:g.55963_56031del

Transcript Alleles

HGVS Amino-acid Change
NM_152291.3:c.710_778del MANE Select NP_689504.2:p.Ala237_Ala259del
ENST00000304887.6:c.710_778del MANE Select ENSP00000302021.5:p.Ala237_Ala259del
NM_001145006.1:c.710_778del NP_001138478.1:p.Ala237_Ala259del
NM_001145006.2:c.710_778del NP_001138478.1:p.Ala237_Ala259del
NM_001145007.1:c.710_778del NP_001138479.1:p.Ala237_Ala259del
NM_001145007.2:c.710_778del NP_001138479.1:p.Ala237_Ala259del
NM_152291.2:c.710_778del NP_689504.2:p.Ala237_Ala259del
ENST00000304887.5:c.710_778del ENSP00000302021.5:p.Ala237_Ala259del
ENST00000413702.5:c.710_778del ENSP00000407422.1:p.Ala237_Ala259del
ENST00000456088.5:c.710_778del ENSP00000400585.1:p.Ala237_Ala259del