Canonical Allele Identifier: CA2535233250
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459004_49459005insCC , CM000668.2:g.49459004_49459005insCC GRCh38
NC_000006.11:g.49426717_49426718insCC , CM000668.1:g.49426717_49426718insCC GRCh37
NC_000006.10:g.49534676_49534677insCC NCBI36
NG_007100.1:g.9135_9136insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.385+77_385+78insGG MANE Select ENSP00000274813.3:n.385+77_385+78insGG
ENST00000274813.3:c.385+77_385+78insGG ENSP00000274813.3:n.385+77_385+78insGG
NM_000255.3:c.385+77_385+78insGG NP_000246.2:n.385+77_385+78insGG
XM_005249143.2:c.385+77_385+78insGG XP_005249200.1:n.385+77_385+78insGG
XM_005249143.3:c.385+77_385+78insGG XP_005249200.1:n.385+77_385+78insGG
NM_000255.4:c.385+77_385+78insGG MANE Select NP_000246.2:n.385+77_385+78insGG