Canonical Allele Identifier: CA2549881772
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49444467_49444468insTTATGACAGA , CM000668.2:g.49444467_49444468insTTATGACAGA GRCh38
NC_000006.11:g.49412180_49412181insTTATGACAGA , CM000668.1:g.49412180_49412181insTTATGACAGA GRCh37
NC_000006.10:g.49520139_49520140insTTATGACAGA NCBI36
NG_007100.1:g.23672_23673insTCTGTCATAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1676+171_1676+172insTCTGTCATAA MANE Select ENSP00000274813.3:n.1676+171_1676+172insTCTGTCATAA
ENST00000274813.3:c.1676+171_1676+172insTCTGTCATAA ENSP00000274813.3:n.1676+171_1676+172insTCTGTCATAA
NM_000255.3:c.1676+171_1676+172insTCTGTCATAA NP_000246.2:n.1676+171_1676+172insTCTGTCATAA
XM_005249143.2:c.1676+171_1676+172insTCTGTCATAA XP_005249200.1:n.1676+171_1676+172insTCTGTCATAA
XM_005249143.3:c.1676+171_1676+172insTCTGTCATAA XP_005249200.1:n.1676+171_1676+172insTCTGTCATAA
NM_000255.4:c.1676+171_1676+172insTCTGTCATAA MANE Select NP_000246.2:n.1676+171_1676+172insTCTGTCATAA