Canonical Allele Identifier: CA2679047398

Gene: MMUT

Linked Data

• gnomAD v4: 6-49459437-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459437_49459438insG , CM000668.2:g.49459437_49459438insG	GRCh38
NC_000006.11:g.49427150_49427151insG , CM000668.1:g.49427150_49427151insG	GRCh37
NC_000006.10:g.49535109_49535110insG	NCBI36
NG_007100.1:g.8702_8703insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.29_30insC MANE Select	ENSP00000274813.3:p.Leu10PhefsTer?
ENST00000274813.3:c.29_30insC	ENSP00000274813.3:p.Leu10PhefsTer?
NM_000255.3:c.29_30insC	NP_000246.2:p.Leu10PhefsTer?
XM_005249143.2:c.29_30insC	XP_005249200.1:p.Leu10PhefsTer?
XM_005249143.3:c.29_30insC	XP_005249200.1:p.Leu10PhefsTer?
NM_000255.4:c.29_30insC MANE Select	NP_000246.2:p.Leu10PhefsTer?