Canonical Allele Identifier: CA364405358
Gene: MMUT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459259T>C , CM000668.2:g.49459259T>C GRCh38
NC_000006.11:g.49426972T>C , CM000668.1:g.49426972T>C GRCh37
NC_000006.10:g.49534931T>C NCBI36
NG_007100.1:g.8881A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.208A>G MANE Select ENSP00000274813.3:p.Lys70Glu
ENST00000274813.3:c.208A>G ENSP00000274813.3:p.Lys70Glu
NM_000255.3:c.208A>G NP_000246.2:p.Lys70Glu
XM_005249143.2:c.208A>G XP_005249200.1:p.Lys70Glu
XM_005249143.3:c.208A>G XP_005249200.1:p.Lys70Glu
NM_000255.4:c.208A>G MANE Select NP_000246.2:p.Lys70Glu