Canonical Allele Identifier: CA364397284
Gene: MMUT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447770A>C , CM000668.2:g.49447770A>C GRCh38
NC_000006.11:g.49415483A>C , CM000668.1:g.49415483A>C GRCh37
NC_000006.10:g.49523442A>C NCBI36
NG_007100.1:g.20370T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1460T>G MANE Select ENSP00000274813.3:p.Val487Gly
ENST00000274813.3:c.1460T>G ENSP00000274813.3:p.Val487Gly
NM_000255.3:c.1460T>G NP_000246.2:p.Val487Gly
XM_005249143.2:c.1460T>G XP_005249200.1:p.Val487Gly
XM_005249143.3:c.1460T>G XP_005249200.1:p.Val487Gly
NM_000255.4:c.1460T>G MANE Select NP_000246.2:p.Val487Gly