Canonical Allele Identifier: CA2410907927
Gene: TYMP HGNC NCBI

Linked Data

dbSNP Id: rs2069385920

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50526501_50526514del , CM000684.2:g.50526501_50526514del GRCh38
NC_000022.10:g.50964930_50964943del , CM000684.1:g.50964930_50964943del GRCh37
NC_000022.9:g.49311796_49311809del NCBI36
NG_011860.1:g.8574_8587del , LRG_727:g.8574_8587del
NG_016235.1:g.4928_4941del
NG_021419.1:g.23286_23299del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252029.8:c.929-36_929-23del MANE Select ENSP00000252029.3:n.929-36_929-23del
ENST00000395680.6:c.929-36_929-23del ENSP00000379037.1:n.929-36_929-23del
ENST00000395681.6:c.929-36_929-23del ENSP00000379038.1:n.929-36_929-23del
ENST00000650719.1:c.810-36_810-23del ENSP00000498276.1:n.810-36_810-23del
ENST00000651401.1:c.413-36_413-23del ENSP00000499115.1:n.413-36_413-23del
ENST00000652401.1:c.430-36_430-23del
ENST00000252029.7:c.929-36_929-23del ENSP00000252029.3:n.929-36_929-23del
ENST00000395678.7:c.929-36_929-23del ENSP00000379036.3:n.929-36_929-23del
ENST00000395680.5:c.929-36_929-23del ENSP00000379037.1:n.929-36_929-23del
ENST00000395681.5:c.929-36_929-23del ENSP00000379038.1:n.929-36_929-23del
ENST00000425169.1:c.830-36_830-23del ENSP00000395875.1:n.830-36_830-23del
ENST00000476284.1:n.935-36_935-23del
ENST00000487577.5:n.1216-36_1216-23del
NM_001113755.2:c.929-36_929-23del NP_001107227.1:n.929-36_929-23del
NM_001113756.2:c.929-36_929-23del NP_001107228.1:n.929-36_929-23del
NM_001257988.1:c.929-36_929-23del , LRG_727t1:c.929-36_929-23del NP_001244917.1:n.929-36_929-23del
NM_001257989.1:c.929-36_929-23del , LRG_727t2:c.929-36_929-23del NP_001244918.1:n.929-36_929-23del
NM_001953.4:c.929-36_929-23del NP_001944.1:n.929-36_929-23del
NM_001113755.3:c.929-36_929-23del NP_001107227.1:n.929-36_929-23del
NM_001113756.3:c.929-36_929-23del NP_001107228.1:n.929-36_929-23del
NM_001953.5:c.929-36_929-23del MANE Select NP_001944.1:n.929-36_929-23del