Canonical Allele Identifier: CA364397302

Gene: MMUT

Linked Data

• MyVariant Identifiers: chr6:g.49415491T>A (hg19) ; chr6:g.49447778T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49447778T>A , CM000668.2:g.49447778T>A	GRCh38
NC_000006.11:g.49415491T>A , CM000668.1:g.49415491T>A	GRCh37
NC_000006.10:g.49523450T>A	NCBI36
NG_007100.1:g.20362A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1452A>T MANE Select	ENSP00000274813.3:p.Glu484Asp
ENST00000274813.3:c.1452A>T	ENSP00000274813.3:p.Glu484Asp
NM_000255.3:c.1452A>T	NP_000246.2:p.Glu484Asp
XM_005249143.2:c.1452A>T	XP_005249200.1:p.Glu484Asp
XM_005249143.3:c.1452A>T	XP_005249200.1:p.Glu484Asp
NM_000255.4:c.1452A>T MANE Select	NP_000246.2:p.Glu484Asp