Canonical Allele Identifier: CA2770993549
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49458134T>C , CM000668.2:g.49458134T>C GRCh38
NC_000006.11:g.49425847T>C , CM000668.1:g.49425847T>C GRCh37
NC_000006.10:g.49533806T>C NCBI36
NG_007100.1:g.10006A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.386-76A>G MANE Select ENSP00000274813.3:n.386-76A>G
ENST00000274813.3:c.386-76A>G ENSP00000274813.3:n.386-76A>G
NM_000255.3:c.386-76A>G NP_000246.2:n.386-76A>G
XM_005249143.2:c.386-76A>G XP_005249200.1:n.386-76A>G
XM_005249143.3:c.386-76A>G XP_005249200.1:n.386-76A>G
NM_000255.4:c.386-76A>G MANE Select NP_000246.2:n.386-76A>G