Canonical Allele Identifier: CA2410909527

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529095T= , CM000684.2:g.50529095T=	GRCh38
NC_000022.10:g.50967524T= , CM000684.1:g.50967524T=	GRCh37
NC_000022.9:g.49314390T=	NCBI36
NG_011860.1:g.5991A= , LRG_727:g.5991A=
NG_016235.1:g.2345A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252029.8:c.417+41A= MANE Select	ENSP00000252029.3:n.417+41A=
ENST00000395680.6:c.417+41A=	ENSP00000379037.1:n.417+41A=
ENST00000395681.6:c.417+41A=	ENSP00000379038.1:n.417+41A=
ENST00000650719.1:c.417+41A=	ENSP00000498276.1:n.417+41A=
ENST00000651095.1:n.597A=
ENST00000651401.1:c.-1+809A=	ENSP00000499115.1:n.-1+809A=
ENST00000651906.1:n.536+41A=
ENST00000652237.1:n.734A=
ENST00000652352.1:c.165+41A=	ENSP00000498579.1:n.165+41A=
ENST00000252029.7:c.417+41A=	ENSP00000252029.3:n.417+41A=
ENST00000395678.7:c.417+41A=	ENSP00000379036.3:n.417+41A=
ENST00000395680.5:c.417+41A=	ENSP00000379037.1:n.417+41A=
ENST00000395681.5:c.417+41A=	ENSP00000379038.1:n.417+41A=
ENST00000425169.1:c.417+41A=	ENSP00000395875.1:n.417+41A=
ENST00000476284.1:n.542+41A=
ENST00000487162.1:n.746A=
ENST00000487577.5:n.704+41A=
NM_001113755.2:c.417+41A=	NP_001107227.1:n.417+41A=
NM_001113756.2:c.417+41A=	NP_001107228.1:n.417+41A=
NM_001257988.1:c.417+41A= , LRG_727t1:c.417+41A=	NP_001244917.1:n.417+41A=
NM_001257989.1:c.417+41A= , LRG_727t2:c.417+41A=	NP_001244918.1:n.417+41A=
NM_001953.4:c.417+41A=	NP_001944.1:n.417+41A=
NM_001113755.3:c.417+41A=	NP_001107227.1:n.417+41A=
NM_001113756.3:c.417+41A=	NP_001107228.1:n.417+41A=
NM_001953.5:c.417+41A= MANE Select	NP_001944.1:n.417+41A=