Canonical Allele Identifier: CA2410909724

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529441_50529454delinsTCTCTCGGGCTGAC , CM000684.2:g.50529441_50529454delinsTCTCTCGGGCTGAC	GRCh38
NC_000022.10:g.50967870_50967883delinsTCTCTCGGGCTGAC , CM000684.1:g.50967870_50967883delinsTCTCTCGGGCTGAC	GRCh37
NC_000022.9:g.49314736_49314749delinsTCTCTCGGGCTGAC	NCBI36
NG_011860.1:g.5632_5645delinsGTCAGCCCGAGAGA , LRG_727:g.5632_5645delinsGTCAGCCCGAGAGA
NG_016235.1:g.1986_1999delinsGTCAGCCCGAGAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.214+42_214+55delinsGTCAGCCCGAGAGA MANE Select	ENSP00000252029.3:n.214+42_214+55delinsGTCAGCCCGAGAGA
ENST00000395680.6:c.214+42_214+55delinsGTCAGCCCGAGAGA	ENSP00000379037.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
ENST00000395681.6:c.214+42_214+55delinsGTCAGCCCGAGAGA	ENSP00000379038.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
ENST00000650719.1:c.214+42_214+55delinsGTCAGCCCGAGAGA	ENSP00000498276.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
ENST00000651095.1:n.353+42_353+55delinsGTCAGCCCGAGAGA
ENST00000651196.1:c.214+42_214+55delinsGTCAGCCCGAGAGA	ENSP00000499096.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
ENST00000651401.1:c.-1+450_-1+463delinsGTCAGCCCGAGAGA	ENSP00000499115.1:n.-1+450_-1+463delinsGTCAGCCCGAGAGA
ENST00000651906.1:n.333+42_333+55delinsGTCAGCCCGAGAGA
ENST00000652237.1:n.375_388delinsGTCAGCCCGAGAGA
ENST00000252029.7:c.214+42_214+55delinsGTCAGCCCGAGAGA	ENSP00000252029.3:n.214+42_214+55delinsGTCAGCCCGAGAGA
ENST00000395678.7:c.214+42_214+55delinsGTCAGCCCGAGAGA	ENSP00000379036.3:n.214+42_214+55delinsGTCAGCCCGAGAGA
ENST00000395680.5:c.214+42_214+55delinsGTCAGCCCGAGAGA	ENSP00000379037.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
ENST00000395681.5:c.214+42_214+55delinsGTCAGCCCGAGAGA	ENSP00000379038.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
ENST00000425169.1:c.214+42_214+55delinsGTCAGCCCGAGAGA	ENSP00000395875.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
ENST00000476284.1:n.339+42_339+55delinsGTCAGCCCGAGAGA
ENST00000487162.1:n.387_400delinsGTCAGCCCGAGAGA
ENST00000487577.5:n.501+42_501+55delinsGTCAGCCCGAGAGA
NM_001113755.2:c.214+42_214+55delinsGTCAGCCCGAGAGA	NP_001107227.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
NM_001113756.2:c.214+42_214+55delinsGTCAGCCCGAGAGA	NP_001107228.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
NM_001257988.1:c.214+42_214+55delinsGTCAGCCCGAGAGA , LRG_727t1:c.214+42_214+55delinsGTCAGCCCGAGAGA	NP_001244917.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
NM_001257989.1:c.214+42_214+55delinsGTCAGCCCGAGAGA , LRG_727t2:c.214+42_214+55delinsGTCAGCCCGAGAGA	NP_001244918.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
NM_001953.4:c.214+42_214+55delinsGTCAGCCCGAGAGA	NP_001944.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
NM_001113755.3:c.214+42_214+55delinsGTCAGCCCGAGAGA	NP_001107227.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
NM_001113756.3:c.214+42_214+55delinsGTCAGCCCGAGAGA	NP_001107228.1:n.214+42_214+55delinsGTCAGCCCGAGAGA
NM_001953.5:c.214+42_214+55delinsGTCAGCCCGAGAGA MANE Select	NP_001944.1:n.214+42_214+55delinsGTCAGCCCGAGAGA