Canonical Allele Identifier: CA1627395623

Gene: MMUT

Linked Data

• dbSNP Id: rs1767740279

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49458077_49458078insAAAAAAAA , CM000668.2:g.49458077_49458078insAAAAAAAA	GRCh38
NC_000006.11:g.49425790_49425791insAAAAAAAA , CM000668.1:g.49425790_49425791insAAAAAAAA	GRCh37
NC_000006.10:g.49533749_49533750insAAAAAAAA	NCBI36
NG_007100.1:g.10067_10068insTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.386-15_386-14insTTTTTTTT MANE Select	ENSP00000274813.3:n.386-15_386-14insTTTTTTTT
ENST00000274813.3:c.386-15_386-14insTTTTTTTT	ENSP00000274813.3:n.386-15_386-14insTTTTTTTT
NM_000255.3:c.386-15_386-14insTTTTTTTT	NP_000246.2:n.386-15_386-14insTTTTTTTT
XM_005249143.2:c.386-15_386-14insTTTTTTTT	XP_005249200.1:n.386-15_386-14insTTTTTTTT
XM_005249143.3:c.386-15_386-14insTTTTTTTT	XP_005249200.1:n.386-15_386-14insTTTTTTTT
NM_000255.4:c.386-15_386-14insTTTTTTTT MANE Select	NP_000246.2:n.386-15_386-14insTTTTTTTT