Canonical Allele Identifier: CA917744659

Gene: MMUT

Linked Data

• dbSNP Id: rs869098825

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459052_49459053del , CM000668.2:g.49459052_49459053del	GRCh38
NC_000006.11:g.49426765_49426766del , CM000668.1:g.49426765_49426766del	GRCh37
NC_000006.10:g.49534724_49534725del	NCBI36
NG_007100.1:g.9088_9089del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.385+30_385+31del MANE Select	ENSP00000274813.3:n.385+30_385+31del
ENST00000274813.3:c.385+30_385+31del	ENSP00000274813.3:n.385+30_385+31del
NM_000255.3:c.385+30_385+31del	NP_000246.2:n.385+30_385+31del
XM_005249143.2:c.385+30_385+31del	XP_005249200.1:n.385+30_385+31del
XM_005249143.3:c.385+30_385+31del	XP_005249200.1:n.385+30_385+31del
NM_000255.4:c.385+30_385+31del MANE Select	NP_000246.2:n.385+30_385+31del