Canonical Allele Identifier: CA364404613
Gene: MMUT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49457951C>A , CM000668.2:g.49457951C>A GRCh38
NC_000006.11:g.49425664C>A , CM000668.1:g.49425664C>A GRCh37
NC_000006.10:g.49533623C>A NCBI36
NG_007100.1:g.10189G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.493G>T MANE Select ENSP00000274813.3:p.Asp165Tyr
ENST00000274813.3:c.493G>T ENSP00000274813.3:p.Asp165Tyr
NM_000255.3:c.493G>T NP_000246.2:p.Asp165Tyr
XM_005249143.2:c.493G>T XP_005249200.1:p.Asp165Tyr
XM_005249143.3:c.493G>T XP_005249200.1:p.Asp165Tyr
NM_000255.4:c.493G>T MANE Select NP_000246.2:p.Asp165Tyr