Canonical Allele Identifier: CA364404880
Gene: MMUT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459094C>A , CM000668.2:g.49459094C>A GRCh38
NC_000006.11:g.49426807C>A , CM000668.1:g.49426807C>A GRCh37
NC_000006.10:g.49534766C>A NCBI36
NG_007100.1:g.9046G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.373G>T MANE Select ENSP00000274813.3:p.Asp125Tyr
ENST00000274813.3:c.373G>T ENSP00000274813.3:p.Asp125Tyr
NM_000255.3:c.373G>T NP_000246.2:p.Asp125Tyr
XM_005249143.2:c.373G>T XP_005249200.1:p.Asp125Tyr
XM_005249143.3:c.373G>T XP_005249200.1:p.Asp125Tyr
NM_000255.4:c.373G>T MANE Select NP_000246.2:p.Asp125Tyr