Canonical Allele Identifier: CA650898859
Gene: MMUT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49458083dup , CM000668.2:g.49458083dup GRCh38
NC_000006.11:g.49425796dup , CM000668.1:g.49425796dup GRCh37
NC_000006.10:g.49533755dup NCBI36
NG_007100.1:g.10057dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.386-25dup MANE Select ENSP00000274813.3:n.386-25dup
ENST00000274813.3:c.386-25dup ENSP00000274813.3:n.386-25dup
NM_000255.3:c.386-25dup NP_000246.2:n.386-25dup
XM_005249143.2:c.386-25dup XP_005249200.1:n.386-25dup
XM_005249143.3:c.386-25dup XP_005249200.1:n.386-25dup
NM_000255.4:c.386-25dup MANE Select NP_000246.2:n.386-25dup