Canonical Allele Identifier: CA2679047386

Gene: MMUT

Linked Data

• gnomAD v4: 6-49457657-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49457660_49457661del , CM000668.2:g.49457660_49457661del	GRCh38
NC_000006.11:g.49425373_49425374del , CM000668.1:g.49425373_49425374del	GRCh37
NC_000006.10:g.49533332_49533333del	NCBI36
NG_007100.1:g.10481_10482del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.753+32_753+33del MANE Select	ENSP00000274813.3:n.753+32_753+33del
ENST00000274813.3:c.753+32_753+33del	ENSP00000274813.3:n.753+32_753+33del
NM_000255.3:c.753+32_753+33del	NP_000246.2:n.753+32_753+33del
XM_005249143.2:c.753+32_753+33del	XP_005249200.1:n.753+32_753+33del
XM_005249143.3:c.753+32_753+33del	XP_005249200.1:n.753+32_753+33del
NM_000255.4:c.753+32_753+33del MANE Select	NP_000246.2:n.753+32_753+33del