Canonical Allele Identifier: CA212988

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529138_50529340del , CM000684.2:g.50529138_50529340del	GRCh38
NC_000022.10:g.50967567_50967769del , CM000684.1:g.50967567_50967769del	GRCh37
NC_000022.9:g.49314433_49314635del	NCBI36
NG_011860.1:g.5749_5951del , LRG_727:g.5749_5951del
NG_016235.1:g.2103_2305del

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.216_417+1del
ENST00000395680.6:c.216_417+1del
ENST00000395681.6:c.216_417+1del
ENST00000650719.1:c.216_417+1del
ENST00000651095.1:n.355_557del
ENST00000651401.1:c.-1+567_-1+769del	ENSP00000499115.1:n.-1+567_-1+769del
ENST00000651906.1:n.335_536+1del
ENST00000652237.1:n.492_694del
ENST00000252029.7:c.216_417+1del
ENST00000395678.7:c.216_417+1del
ENST00000395680.5:c.216_417+1del
ENST00000395681.5:c.216_417+1del
ENST00000425169.1:c.216_417+1del
ENST00000476284.1:n.341_542+1del
ENST00000487162.1:n.504_706del
ENST00000487577.5:n.503_704+1del
NM_001113755.2:c.216_417+1del
NM_001113756.2:c.216_417+1del
NM_001257988.1:c.216_417+1del , LRG_727t1:c.216_417+1del
NM_001257989.1:c.216_417+1del , LRG_727t2:c.216_417+1del
NM_001953.4:c.216_417+1del
NM_001113755.3:c.216_417+1del
NM_001113756.3:c.216_417+1del
NM_001953.5:c.216_417+1del