Canonical Allele Identifier: CA2410908697

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50527640T= , CM000684.2:g.50527640T=	GRCh38
NC_000022.10:g.50966069T= , CM000684.1:g.50966069T=	GRCh37
NC_000022.9:g.49312935T=	NCBI36
NG_011860.1:g.7446A= , LRG_727:g.7446A=
NG_016235.1:g.3800A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.594A= MANE Select	ENSP00000252029.3:p.Leu198=
ENST00000395680.6:c.594A=	ENSP00000379037.1:p.Leu198=
ENST00000395681.6:c.594A=	ENSP00000379038.1:p.Leu198=
ENST00000650719.1:c.594A=	ENSP00000498276.1:p.Leu198=
ENST00000651401.1:c.78A=	ENSP00000499115.1:p.Leu26=
ENST00000651906.1:n.713A=
ENST00000652352.1:c.305A=	ENSP00000498579.1:p.Tyr102=
ENST00000652401.1:c.50A=
ENST00000252029.7:c.594A=	ENSP00000252029.3:p.Leu198=
ENST00000395678.7:c.594A=	ENSP00000379036.3:p.Leu198=
ENST00000395680.5:c.594A=	ENSP00000379037.1:p.Leu198=
ENST00000395681.5:c.594A=	ENSP00000379038.1:p.Leu198=
ENST00000425169.1:c.495A=	ENSP00000395875.1:p.Leu165=
ENST00000476284.1:n.719A=
ENST00000487577.5:n.881A=
NM_001113755.2:c.594A=	NP_001107227.1:p.Leu198=
NM_001113756.2:c.594A=	NP_001107228.1:p.Leu198=
NM_001257988.1:c.594A= , LRG_727t1:c.594A=	NP_001244917.1:p.Leu198=
NM_001257989.1:c.594A= , LRG_727t2:c.594A=	NP_001244918.1:p.Leu198=
NM_001953.4:c.594A=	NP_001944.1:p.Leu198=
NM_001113755.3:c.594A=	NP_001107227.1:p.Leu198=
NM_001113756.3:c.594A=	NP_001107228.1:p.Leu198=
NM_001953.5:c.594A= MANE Select	NP_001944.1:p.Leu198=