Canonical Allele Identifier: CA2279748806
Community Standard Title: NM_001071.4(TYMS):c.279+115A=
Gene: TYMS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.659829A= , CM000680.2:g.659829A= GRCh38
NC_000018.9:g.659829A= , CM000680.1:g.659829A= GRCh37
NC_000018.8:g.649829A= NCBI36
NG_028255.1:g.7226A= , LRG_783:g.7226A=

Transcript Alleles

HGVS Amino-acid Change
NM_001071.4:c.279+115A= MANE Select NP_001062.1:n.279+115A=
ENST00000323274.15:c.279+115A= MANE Select ENSP00000315644.10:n.279+115A=
NM_001071.2:c.279+115A= , LRG_783t1:c.279+115A= NP_001062.1:n.279+115A=
NM_001071.3:c.279+115A= NP_001062.1:n.279+115A=
NM_001354867.1:c.279+115A= NP_001341796.1:n.279+115A=
NM_001354867.2:c.279+115A= NP_001341796.1:n.279+115A=
NM_001354868.1:c.205+1882A= NP_001341797.1:n.205+1882A=
NM_001354868.2:c.205+1882A= NP_001341797.1:n.205+1882A=
ENST00000323224.7:c.279+115A= ENSP00000314727.7:n.279+115A=
ENST00000323250.9:c.205+1882A= ENSP00000314902.5:n.205+1882A=
ENST00000323274.14:c.279+115A= ENSP00000315644.10:n.279+115A=
ENST00000579128.1:n.357+115A=