Canonical Allele Identifier: CA697115151

Gene: MTUS2

Linked Data

• dbSNP Id: rs2479768
• MyVariant Identifiers: chr13:g.29620654A>T (hg19) ; chr13:g.29046517A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.29046517A>T , CM000675.2:g.29046517A>T	GRCh38
NC_000013.10:g.29620654A>T , CM000675.1:g.29620654A>T	GRCh37
NC_000013.9:g.28518654A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000612955.6:c.2446+12392A>T MANE Select	ENSP00000483729.2:n.2446+12392A>T
ENST00000431530.7:c.2476+12392A>T	ENSP00000392057.3:n.2476+12392A>T
ENST00000612955.4:c.2476+12392A>T	ENSP00000483729.1:n.2476+12392A>T
NM_001033602.2:c.2476+12392A>T	NP_001028774.2:n.2476+12392A>T
XM_011535019.1:c.2476+12392A>T	XP_011533321.1:n.2476+12392A>T
XM_011535020.1:c.2476+12392A>T	XP_011533322.1:n.2476+12392A>T
XM_011535021.1:c.2476+12392A>T	XP_011533323.1:n.2476+12392A>T
XM_011535022.1:c.-25+12392A>T	XP_011533324.1:n.-25+12392A>T
XM_011535023.1:c.-28+12392A>T	XP_011533325.1:n.-28+12392A>T
NM_001033602.3:c.2446+12392A>T	NP_001028774.3:n.2446+12392A>T
NM_001366650.1:c.2446+12392A>T	NP_001353579.1:n.2446+12392A>T
NM_001366651.1:c.2446+12392A>T	NP_001353580.1:n.2446+12392A>T
XM_011535019.3:c.2476+12392A>T	XP_011533321.1:n.2476+12392A>T
XM_011535020.3:c.2476+12392A>T	XP_011533322.1:n.2476+12392A>T
XM_011535022.2:c.-25+12392A>T	XP_011533324.1:n.-25+12392A>T
XM_017020500.2:c.2476+12392A>T	XP_016875989.1:n.2476+12392A>T
XM_017020501.2:c.2476+12392A>T	XP_016875990.1:n.2476+12392A>T
XM_024449335.1:c.-28+12392A>T	XP_024305103.1:n.-28+12392A>T
NM_001033602.4:c.2446+12392A>T MANE Select	NP_001028774.3:n.2446+12392A>T
NM_001384605.1:c.2446+12392A>T	NP_001371534.1:n.2446+12392A>T
NM_001384606.1:c.2446+12392A>T	NP_001371535.1:n.2446+12392A>T