Canonical Allele Identifier: CA2657568390

Gene: TYMP

Linked Data

• gnomAD v4: 22-50529490-A-ACG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529492_50529493dup , CM000684.2:g.50529492_50529493dup	GRCh38
NC_000022.10:g.50967921_50967922dup , CM000684.1:g.50967921_50967922dup	GRCh37
NC_000022.9:g.49314787_49314788dup	NCBI36
NG_011860.1:g.5594_5595dup , LRG_727:g.5594_5595dup
NG_016235.1:g.1948_1949dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.214+4_214+5dup MANE Select	ENSP00000252029.3:n.214+4_214+5dup
ENST00000395680.6:c.214+4_214+5dup	ENSP00000379037.1:n.214+4_214+5dup
ENST00000395681.6:c.214+4_214+5dup	ENSP00000379038.1:n.214+4_214+5dup
ENST00000650719.1:c.214+4_214+5dup	ENSP00000498276.1:n.214+4_214+5dup
ENST00000651095.1:n.353+4_353+5dup
ENST00000651196.1:c.214+4_214+5dup	ENSP00000499096.1:n.214+4_214+5dup
ENST00000651401.1:c.-1+412_-1+413dup	ENSP00000499115.1:n.-1+412_-1+413dup
ENST00000651906.1:n.333+4_333+5dup
ENST00000652237.1:n.337_338dup
ENST00000252029.7:c.214+4_214+5dup	ENSP00000252029.3:n.214+4_214+5dup
ENST00000395678.7:c.214+4_214+5dup	ENSP00000379036.3:n.214+4_214+5dup
ENST00000395680.5:c.214+4_214+5dup	ENSP00000379037.1:n.214+4_214+5dup
ENST00000395681.5:c.214+4_214+5dup	ENSP00000379038.1:n.214+4_214+5dup
ENST00000425169.1:c.214+4_214+5dup	ENSP00000395875.1:n.214+4_214+5dup
ENST00000476284.1:n.339+4_339+5dup
ENST00000487162.1:n.349_350dup
ENST00000487577.5:n.501+4_501+5dup
NM_001113755.2:c.214+4_214+5dup	NP_001107227.1:n.214+4_214+5dup
NM_001113756.2:c.214+4_214+5dup	NP_001107228.1:n.214+4_214+5dup
NM_001257988.1:c.214+4_214+5dup , LRG_727t1:c.214+4_214+5dup	NP_001244917.1:n.214+4_214+5dup
NM_001257989.1:c.214+4_214+5dup , LRG_727t2:c.214+4_214+5dup	NP_001244918.1:n.214+4_214+5dup
NM_001953.4:c.214+4_214+5dup	NP_001944.1:n.214+4_214+5dup
NM_001113755.3:c.214+4_214+5dup	NP_001107227.1:n.214+4_214+5dup
NM_001113756.3:c.214+4_214+5dup	NP_001107228.1:n.214+4_214+5dup
NM_001953.5:c.214+4_214+5dup MANE Select	NP_001944.1:n.214+4_214+5dup