Canonical Allele Identifier: CA364397289
Gene: MMUT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447772A>C , CM000668.2:g.49447772A>C GRCh38
NC_000006.11:g.49415485A>C , CM000668.1:g.49415485A>C GRCh37
NC_000006.10:g.49523444A>C NCBI36
NG_007100.1:g.20368T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1458T>G MANE Select ENSP00000274813.3:p.Ile486Met
ENST00000274813.3:c.1458T>G ENSP00000274813.3:p.Ile486Met
NM_000255.3:c.1458T>G NP_000246.2:p.Ile486Met
XM_005249143.2:c.1458T>G XP_005249200.1:p.Ile486Met
XM_005249143.3:c.1458T>G XP_005249200.1:p.Ile486Met
NM_000255.4:c.1458T>G MANE Select NP_000246.2:p.Ile486Met