Canonical Allele Identifier: CA450398232

Gene: MMUT

Linked Data

• MyVariant Identifiers: chr6:g.49415482A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49447769A>T , CM000668.2:g.49447769A>T	GRCh38
NC_000006.11:g.49415482A>T , CM000668.1:g.49415482A>T	GRCh37
NC_000006.10:g.49523441A>T	NCBI36
NG_007100.1:g.20371T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1461T>A MANE Select	ENSP00000274813.3:p.Val487=
ENST00000274813.3:c.1461T>A	ENSP00000274813.3:p.Val487=
NM_000255.3:c.1461T>A	NP_000246.2:p.Val487=
XM_005249143.2:c.1461T>A	XP_005249200.1:p.Val487=
XM_005249143.3:c.1461T>A	XP_005249200.1:p.Val487=
NM_000255.4:c.1461T>A MANE Select	NP_000246.2:p.Val487=