Canonical Allele Identifier: CA2679047385

Gene: MMUT

Linked Data

• gnomAD v4: 6-49457657-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49457657_49457658insA , CM000668.2:g.49457657_49457658insA	GRCh38
NC_000006.11:g.49425370_49425371insA , CM000668.1:g.49425370_49425371insA	GRCh37
NC_000006.10:g.49533329_49533330insA	NCBI36
NG_007100.1:g.10482_10483insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.753+33_753+34insT MANE Select	ENSP00000274813.3:n.753+33_753+34insT
ENST00000274813.3:c.753+33_753+34insT	ENSP00000274813.3:n.753+33_753+34insT
NM_000255.3:c.753+33_753+34insT	NP_000246.2:n.753+33_753+34insT
XM_005249143.2:c.753+33_753+34insT	XP_005249200.1:n.753+33_753+34insT
XM_005249143.3:c.753+33_753+34insT	XP_005249200.1:n.753+33_753+34insT
NM_000255.4:c.753+33_753+34insT MANE Select	NP_000246.2:n.753+33_753+34insT