Canonical Allele Identifier: CA364404552

Gene: MMUT

Linked Data

• MyVariant Identifiers: chr6:g.49425636A>T (hg19) ; chr6:g.49457923A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49457923A>T , CM000668.2:g.49457923A>T	GRCh38
NC_000006.11:g.49425636A>T , CM000668.1:g.49425636A>T	GRCh37
NC_000006.10:g.49533595A>T	NCBI36
NG_007100.1:g.10217T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.521T>A MANE Select	ENSP00000274813.3:p.Phe174Tyr
ENST00000274813.3:c.521T>A	ENSP00000274813.3:p.Phe174Tyr
NM_000255.3:c.521T>A	NP_000246.2:p.Phe174Tyr
XM_005249143.2:c.521T>A	XP_005249200.1:p.Phe174Tyr
XM_005249143.3:c.521T>A	XP_005249200.1:p.Phe174Tyr
NM_000255.4:c.521T>A MANE Select	NP_000246.2:p.Phe174Tyr