Canonical Allele Identifier: CA515387936

Gene: TYMP

Linked Data

• gnomAD v4: 22-50526658-G-C
• MyVariant Identifiers: chr22:g.50965087G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50526658G>C , CM000684.2:g.50526658G>C	GRCh38
NC_000022.10:g.50965087G>C , CM000684.1:g.50965087G>C	GRCh37
NC_000022.9:g.49311953G>C	NCBI36
NG_011860.1:g.8428C>G , LRG_727:g.8428C>G
NG_016235.1:g.4782C>G
NG_021419.1:g.23443G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.846C>G MANE Select	ENSP00000252029.3:p.Gly282=
ENST00000395680.6:c.846C>G	ENSP00000379037.1:p.Gly282=
ENST00000395681.6:c.846C>G	ENSP00000379038.1:p.Gly282=
ENST00000650719.1:c.727C>G	ENSP00000498276.1:p.Pro243Ala
ENST00000651401.1:c.330C>G	ENSP00000499115.1:p.Gly110=
ENST00000652401.1:c.347C>G
ENST00000252029.7:c.846C>G	ENSP00000252029.3:p.Gly282=
ENST00000395678.7:c.846C>G	ENSP00000379036.3:p.Gly282=
ENST00000395680.5:c.846C>G	ENSP00000379037.1:p.Gly282=
ENST00000395681.5:c.846C>G	ENSP00000379038.1:p.Gly282=
ENST00000425169.1:c.747C>G	ENSP00000395875.1:p.Gly249=
ENST00000476284.1:n.852C>G
ENST00000487577.5:n.1133C>G
NM_001113755.2:c.846C>G	NP_001107227.1:p.Gly282=
NM_001113756.2:c.846C>G	NP_001107228.1:p.Gly282=
NM_001257988.1:c.846C>G , LRG_727t1:c.846C>G	NP_001244917.1:p.Gly282=
NM_001257989.1:c.846C>G , LRG_727t2:c.846C>G	NP_001244918.1:p.Gly282=
NM_001953.4:c.846C>G	NP_001944.1:p.Gly282=
NM_001113755.3:c.846C>G	NP_001107227.1:p.Gly282=
NM_001113756.3:c.846C>G	NP_001107228.1:p.Gly282=
NM_001953.5:c.846C>G MANE Select	NP_001944.1:p.Gly282=