Canonical Allele Identifier: CA825483088

Gene: MMUT

Linked Data

• dbSNP Id: rs1297264651
• MyVariant Identifiers: chr6:g.49425858_49425868del (hg19) ; chr6:g.49458145_49458155del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49458146_49458156del , CM000668.2:g.49458146_49458156del	GRCh38
NC_000006.11:g.49425859_49425869del , CM000668.1:g.49425859_49425869del	GRCh37
NC_000006.10:g.49533818_49533828del	NCBI36
NG_007100.1:g.9985_9995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.386-97_386-87del MANE Select	ENSP00000274813.3:n.386-97_386-87del
ENST00000274813.3:c.386-97_386-87del	ENSP00000274813.3:n.386-97_386-87del
NM_000255.3:c.386-97_386-87del	NP_000246.2:n.386-97_386-87del
XM_005249143.2:c.386-97_386-87del	XP_005249200.1:n.386-97_386-87del
XM_005249143.3:c.386-97_386-87del	XP_005249200.1:n.386-97_386-87del
NM_000255.4:c.386-97_386-87del MANE Select	NP_000246.2:n.386-97_386-87del