Canonical Allele Identifier: CA1627388075

Gene: MMUT

Linked Data

• dbSNP Id: rs1767474357
• gnomAD v4: 6-49448770-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49448775dup , CM000668.2:g.49448775dup	GRCh38
NC_000006.11:g.49416488dup , CM000668.1:g.49416488dup	GRCh37
NC_000006.10:g.49524447dup	NCBI36
NG_007100.1:g.19369dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000274813.4:c.1444+45dup MANE Select	ENSP00000274813.3:n.1444+45dup
ENST00000274813.3:c.1444+45dup	ENSP00000274813.3:n.1444+45dup
NM_000255.3:c.1444+45dup	NP_000246.2:n.1444+45dup
XM_005249143.2:c.1444+45dup	XP_005249200.1:n.1444+45dup
XM_005249143.3:c.1444+45dup	XP_005249200.1:n.1444+45dup
NM_000255.4:c.1444+45dup MANE Select	NP_000246.2:n.1444+45dup