Canonical Allele Identifier: CA2410909713

Gene: TYMP

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50529425C= , CM000684.2:g.50529425C=	GRCh38
NC_000022.10:g.50967854C= , CM000684.1:g.50967854C=	GRCh37
NC_000022.9:g.49314720C=	NCBI36
NG_011860.1:g.5661G= , LRG_727:g.5661G=
NG_016235.1:g.2015G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.214+71G= MANE Select	ENSP00000252029.3:n.214+71G=
ENST00000395680.6:c.214+71G=	ENSP00000379037.1:n.214+71G=
ENST00000395681.6:c.214+71G=	ENSP00000379038.1:n.214+71G=
ENST00000650719.1:c.214+71G=	ENSP00000498276.1:n.214+71G=
ENST00000651095.1:n.353+71G=
ENST00000651196.1:c.214+71G=	ENSP00000499096.1:n.214+71G=
ENST00000651401.1:c.-1+479G=	ENSP00000499115.1:n.-1+479G=
ENST00000651906.1:n.333+71G=
ENST00000652237.1:n.404G=
ENST00000252029.7:c.214+71G=	ENSP00000252029.3:n.214+71G=
ENST00000395678.7:c.214+71G=	ENSP00000379036.3:n.214+71G=
ENST00000395680.5:c.214+71G=	ENSP00000379037.1:n.214+71G=
ENST00000395681.5:c.214+71G=	ENSP00000379038.1:n.214+71G=
ENST00000425169.1:c.214+71G=	ENSP00000395875.1:n.214+71G=
ENST00000476284.1:n.339+71G=
ENST00000487162.1:n.416G=
ENST00000487577.5:n.501+71G=
NM_001113755.2:c.214+71G=	NP_001107227.1:n.214+71G=
NM_001113756.2:c.214+71G=	NP_001107228.1:n.214+71G=
NM_001257988.1:c.214+71G= , LRG_727t1:c.214+71G=	NP_001244917.1:n.214+71G=
NM_001257989.1:c.214+71G= , LRG_727t2:c.214+71G=	NP_001244918.1:n.214+71G=
NM_001953.4:c.214+71G=	NP_001944.1:n.214+71G=
NM_001113755.3:c.214+71G=	NP_001107227.1:n.214+71G=
NM_001113756.3:c.214+71G=	NP_001107228.1:n.214+71G=
NM_001953.5:c.214+71G= MANE Select	NP_001944.1:n.214+71G=