Canonical Allele Identifier: CA2538009532
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49444465_49444466insTT , CM000668.2:g.49444465_49444466insTT GRCh38
NC_000006.11:g.49412178_49412179insTT , CM000668.1:g.49412178_49412179insTT GRCh37
NC_000006.10:g.49520137_49520138insTT NCBI36
NG_007100.1:g.23674_23675insAA

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.1676+173_1676+174insAA MANE Select ENSP00000274813.3:n.1676+173_1676+174insAA
ENST00000274813.3:c.1676+173_1676+174insAA ENSP00000274813.3:n.1676+173_1676+174insAA
NM_000255.3:c.1676+173_1676+174insAA NP_000246.2:n.1676+173_1676+174insAA
XM_005249143.2:c.1676+173_1676+174insAA XP_005249200.1:n.1676+173_1676+174insAA
XM_005249143.3:c.1676+173_1676+174insAA XP_005249200.1:n.1676+173_1676+174insAA
NM_000255.4:c.1676+173_1676+174insAA MANE Select NP_000246.2:n.1676+173_1676+174insAA