Canonical Allele Identifier: CA2679047131

Gene: MMUT

Linked Data

• gnomAD v4: 6-49458165-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49458168_49458169dup , CM000668.2:g.49458168_49458169dup	GRCh38
NC_000006.11:g.49425881_49425882dup , CM000668.1:g.49425881_49425882dup	GRCh37
NC_000006.10:g.49533840_49533841dup	NCBI36
NG_007100.1:g.9973_9974dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.386-109_386-108dup MANE Select	ENSP00000274813.3:n.386-109_386-108dup
ENST00000274813.3:c.386-109_386-108dup	ENSP00000274813.3:n.386-109_386-108dup
NM_000255.3:c.386-109_386-108dup	NP_000246.2:n.386-109_386-108dup
XM_005249143.2:c.386-109_386-108dup	XP_005249200.1:n.386-109_386-108dup
XM_005249143.3:c.386-109_386-108dup	XP_005249200.1:n.386-109_386-108dup
NM_000255.4:c.386-109_386-108dup MANE Select	NP_000246.2:n.386-109_386-108dup