Canonical Allele Identifier: CA364404997
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 2740273
ClinVar RCV Id: RCV003575697
gnomAD v4: 6-49459144-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459144C>A , CM000668.2:g.49459144C>A GRCh38
NC_000006.11:g.49426857C>A , CM000668.1:g.49426857C>A GRCh37
NC_000006.10:g.49534816C>A NCBI36
NG_007100.1:g.8996G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.323G>T MANE Select ENSP00000274813.3:p.Arg108Leu
ENST00000274813.3:c.323G>T ENSP00000274813.3:p.Arg108Leu
NM_000255.3:c.323G>T NP_000246.2:p.Arg108Leu
XM_005249143.2:c.323G>T XP_005249200.1:p.Arg108Leu
XM_005249143.3:c.323G>T XP_005249200.1:p.Arg108Leu
NM_000255.4:c.323G>T MANE Select NP_000246.2:p.Arg108Leu