Canonical Allele Identifier: CA2695206695
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459091dup , CM000668.2:g.49459091dup GRCh38
NC_000006.11:g.49426804dup , CM000668.1:g.49426804dup GRCh37
NC_000006.10:g.49534763dup NCBI36
NG_007100.1:g.9050dup

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.377dup MANE Select ENSP00000274813.3:p.Asn126LysfsTer3
ENST00000274813.3:c.377dup ENSP00000274813.3:p.Asn126LysfsTer3
NM_000255.3:c.377dup NP_000246.2:p.Asn126LysfsTer3
XM_005249143.2:c.377dup XP_005249200.1:p.Asn126LysfsTer3
XM_005249143.3:c.377dup XP_005249200.1:p.Asn126LysfsTer3
NM_000255.4:c.377dup MANE Select NP_000246.2:p.Asn126LysfsTer3