Canonical Allele Identifier: CA2679046433

Gene: MMUT

Linked Data

• gnomAD v4: 6-49447835-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49447835_49447836insG , CM000668.2:g.49447835_49447836insG	GRCh38
NC_000006.11:g.49415548_49415549insG , CM000668.1:g.49415548_49415549insG	GRCh37
NC_000006.10:g.49523507_49523508insG	NCBI36
NG_007100.1:g.20304_20305insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1445-51_1445-50insC MANE Select	ENSP00000274813.3:n.1445-51_1445-50insC
ENST00000274813.3:c.1445-51_1445-50insC	ENSP00000274813.3:n.1445-51_1445-50insC
NM_000255.3:c.1445-51_1445-50insC	NP_000246.2:n.1445-51_1445-50insC
XM_005249143.2:c.1445-51_1445-50insC	XP_005249200.1:n.1445-51_1445-50insC
XM_005249143.3:c.1445-51_1445-50insC	XP_005249200.1:n.1445-51_1445-50insC
NM_000255.4:c.1445-51_1445-50insC MANE Select	NP_000246.2:n.1445-51_1445-50insC