Canonical Allele Identifier: CA2679046499

Gene: MMUT

Linked Data

• gnomAD v4: 6-49447935-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49447935_49447936insAA , CM000668.2:g.49447935_49447936insAA	GRCh38
NC_000006.11:g.49415648_49415649insAA , CM000668.1:g.49415648_49415649insAA	GRCh37
NC_000006.10:g.49523607_49523608insAA	NCBI36
NG_007100.1:g.20204_20205insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1445-151_1445-150insTT MANE Select	ENSP00000274813.3:n.1445-151_1445-150insTT
ENST00000274813.3:c.1445-151_1445-150insTT	ENSP00000274813.3:n.1445-151_1445-150insTT
NM_000255.3:c.1445-151_1445-150insTT	NP_000246.2:n.1445-151_1445-150insTT
XM_005249143.2:c.1445-151_1445-150insTT	XP_005249200.1:n.1445-151_1445-150insTT
XM_005249143.3:c.1445-151_1445-150insTT	XP_005249200.1:n.1445-151_1445-150insTT
NM_000255.4:c.1445-151_1445-150insTT MANE Select	NP_000246.2:n.1445-151_1445-150insTT