Canonical Allele Identifier: CA1627395618

Gene: MMUT

Linked Data

• dbSNP Id: rs1767740224

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49458072_49458074del , CM000668.2:g.49458072_49458074del	GRCh38
NC_000006.11:g.49425785_49425787del , CM000668.1:g.49425785_49425787del	GRCh37
NC_000006.10:g.49533744_49533746del	NCBI36
NG_007100.1:g.10068_10070del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.386-14_386-12del MANE Select	ENSP00000274813.3:n.386-14_386-12del
ENST00000274813.3:c.386-14_386-12del	ENSP00000274813.3:n.386-14_386-12del
NM_000255.3:c.386-14_386-12del	NP_000246.2:n.386-14_386-12del
XM_005249143.2:c.386-14_386-12del	XP_005249200.1:n.386-14_386-12del
XM_005249143.3:c.386-14_386-12del	XP_005249200.1:n.386-14_386-12del
NM_000255.4:c.386-14_386-12del MANE Select	NP_000246.2:n.386-14_386-12del