Canonical Allele Identifier: CA2657566702

Gene: TYMP

Linked Data

• gnomAD v4: 22-50527530-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50527532_50527533del , CM000684.2:g.50527532_50527533del	GRCh38
NC_000022.10:g.50965961_50965962del , CM000684.1:g.50965961_50965962del	GRCh37
NC_000022.9:g.49312827_49312828del	NCBI36
NG_011860.1:g.7554_7555del , LRG_727:g.7554_7555del
NG_016235.1:g.3908_3909del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.646+56_646+57del MANE Select	ENSP00000252029.3:n.646+56_646+57del
ENST00000395680.6:c.646+56_646+57del	ENSP00000379037.1:n.646+56_646+57del
ENST00000395681.6:c.646+56_646+57del	ENSP00000379038.1:n.646+56_646+57del
ENST00000650719.1:c.646+56_646+57del	ENSP00000498276.1:n.646+56_646+57del
ENST00000651401.1:c.130+56_130+57del	ENSP00000499115.1:n.130+56_130+57del
ENST00000651906.1:n.821_822del
ENST00000652352.1:c.357+56_357+57del	ENSP00000498579.1:n.357+56_357+57del
ENST00000652401.1:c.102+56_102+57del
ENST00000252029.7:c.646+56_646+57del	ENSP00000252029.3:n.646+56_646+57del
ENST00000395678.7:c.646+56_646+57del	ENSP00000379036.3:n.646+56_646+57del
ENST00000395680.5:c.646+56_646+57del	ENSP00000379037.1:n.646+56_646+57del
ENST00000395681.5:c.646+56_646+57del	ENSP00000379038.1:n.646+56_646+57del
ENST00000425169.1:c.547+56_547+57del	ENSP00000395875.1:n.547+56_547+57del
ENST00000476284.1:n.771+56_771+57del
ENST00000487577.5:n.933+56_933+57del
NM_001113755.2:c.646+56_646+57del	NP_001107227.1:n.646+56_646+57del
NM_001113756.2:c.646+56_646+57del	NP_001107228.1:n.646+56_646+57del
NM_001257988.1:c.646+56_646+57del , LRG_727t1:c.646+56_646+57del	NP_001244917.1:n.646+56_646+57del
NM_001257989.1:c.646+56_646+57del , LRG_727t2:c.646+56_646+57del	NP_001244918.1:n.646+56_646+57del
NM_001953.4:c.646+56_646+57del	NP_001944.1:n.646+56_646+57del
NM_001113755.3:c.646+56_646+57del	NP_001107227.1:n.646+56_646+57del
NM_001113756.3:c.646+56_646+57del	NP_001107228.1:n.646+56_646+57del
NM_001953.5:c.646+56_646+57del MANE Select	NP_001944.1:n.646+56_646+57del