Canonical Allele Identifier: CA2279751894
Community Standard Title: NM_001071.4(TYMS):c.455-2701G=
Gene: TYMS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.666371G= , CM000680.2:g.666371G= GRCh38
NC_000018.9:g.666371G= , CM000680.1:g.666371G= GRCh37
NC_000018.8:g.656371G= NCBI36
NG_028255.1:g.13768G= , LRG_783:g.13768G=

Transcript Alleles

HGVS Amino-acid Change
NM_001071.4:c.455-2701G= MANE Select NP_001062.1:n.455-2701G=
ENST00000323274.15:c.455-2701G= MANE Select ENSP00000315644.10:n.455-2701G=
NM_001071.2:c.455-2701G= , LRG_783t1:c.455-2701G= NP_001062.1:n.455-2701G=
NM_001071.3:c.455-2701G= NP_001062.1:n.455-2701G=
NM_001354867.1:c.454+4051G= NP_001341796.1:n.454+4051G=
NM_001354867.2:c.454+4051G= NP_001341796.1:n.454+4051G=
NM_001354868.1:c.206-2701G= NP_001341797.1:n.206-2701G=
NM_001354868.2:c.206-2701G= NP_001341797.1:n.206-2701G=
ENST00000323224.7:c.454+4051G= ENSP00000314727.7:n.454+4051G=
ENST00000323250.9:c.206-2701G= ENSP00000314902.5:n.206-2701G=
ENST00000323274.14:c.455-2701G= ENSP00000315644.10:n.455-2701G=
ENST00000579128.1:n.533-2701G=