Canonical Allele Identifier: CA2679047263

Gene: MMUT

Linked Data

• gnomAD v4: 6-49459011-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459016dup , CM000668.2:g.49459016dup	GRCh38
NC_000006.11:g.49426729dup , CM000668.1:g.49426729dup	GRCh37
NC_000006.10:g.49534688dup	NCBI36
NG_007100.1:g.9128dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.385+70dup MANE Select	ENSP00000274813.3:n.385+70dup
ENST00000274813.3:c.385+70dup	ENSP00000274813.3:n.385+70dup
NM_000255.3:c.385+70dup	NP_000246.2:n.385+70dup
XM_005249143.2:c.385+70dup	XP_005249200.1:n.385+70dup
XM_005249143.3:c.385+70dup	XP_005249200.1:n.385+70dup
NM_000255.4:c.385+70dup MANE Select	NP_000246.2:n.385+70dup