Canonical Allele Identifier: CA2679047384

Gene: MMUT

Linked Data

• gnomAD v4: 6-49457655-A-AAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49457656_49457657insATA , CM000668.2:g.49457656_49457657insATA	GRCh38
NC_000006.11:g.49425369_49425370insATA , CM000668.1:g.49425369_49425370insATA	GRCh37
NC_000006.10:g.49533328_49533329insATA	NCBI36
NG_007100.1:g.10484_10485insATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.753+35_753+36insATT MANE Select	ENSP00000274813.3:n.753+35_753+36insATT
ENST00000274813.3:c.753+35_753+36insATT	ENSP00000274813.3:n.753+35_753+36insATT
NM_000255.3:c.753+35_753+36insATT	NP_000246.2:n.753+35_753+36insATT
XM_005249143.2:c.753+35_753+36insATT	XP_005249200.1:n.753+35_753+36insATT
XM_005249143.3:c.753+35_753+36insATT	XP_005249200.1:n.753+35_753+36insATT
NM_000255.4:c.753+35_753+36insATT MANE Select	NP_000246.2:n.753+35_753+36insATT