Canonical Allele Identifier: CA364405242

Gene: MMUT

Linked Data

• gnomAD v4: 6-49459228-T-G
• MyVariant Identifiers: chr6:g.49426941T>G (hg19) ; chr6:g.49459228T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459228T>G , CM000668.2:g.49459228T>G	GRCh38
NC_000006.11:g.49426941T>G , CM000668.1:g.49426941T>G	GRCh37
NC_000006.10:g.49534900T>G	NCBI36
NG_007100.1:g.8912A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.239A>C MANE Select	ENSP00000274813.3:p.Asp80Ala
ENST00000274813.3:c.239A>C	ENSP00000274813.3:p.Asp80Ala
NM_000255.3:c.239A>C	NP_000246.2:p.Asp80Ala
XM_005249143.2:c.239A>C	XP_005249200.1:p.Asp80Ala
XM_005249143.3:c.239A>C	XP_005249200.1:p.Asp80Ala
NM_000255.4:c.239A>C MANE Select	NP_000246.2:p.Asp80Ala