Canonical Allele Identifier: CA2695206698
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459199delinsTT , CM000668.2:g.49459199delinsTT GRCh38
NC_000006.11:g.49426912delinsTT , CM000668.1:g.49426912delinsTT GRCh37
NC_000006.10:g.49534871delinsTT NCBI36
NG_007100.1:g.8941delinsAA

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.268delinsAA MANE Select ENSP00000274813.3:p.Pro90AsnfsTer14
ENST00000274813.3:c.268delinsAA ENSP00000274813.3:p.Pro90AsnfsTer14
NM_000255.3:c.268delinsAA NP_000246.2:p.Pro90AsnfsTer14
XM_005249143.2:c.268delinsAA XP_005249200.1:p.Pro90AsnfsTer14
XM_005249143.3:c.268delinsAA XP_005249200.1:p.Pro90AsnfsTer14
NM_000255.4:c.268delinsAA MANE Select NP_000246.2:p.Pro90AsnfsTer14