Canonical Allele Identifier: CA412197258

Gene: TYMP SCO2

Linked Data

• dbSNP Id: rs773626895
• MyVariant Identifiers: chr22:g.50964678C>G (hg19) ; chr22:g.50526249C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50526249C>G , CM000684.2:g.50526249C>G	GRCh38
NC_000022.10:g.50964678C>G , CM000684.1:g.50964678C>G	GRCh37
NC_000022.9:g.49311544C>G	NCBI36
NG_011860.1:g.8837G>C , LRG_727:g.8837G>C
NG_016235.1:g.5191G>C
NG_021419.1:g.23034C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.1156G>C (TYMP) MANE Select	ENSP00000252029.3:p.Asp386His
ENST00000395680.6:c.1156G>C (TYMP)	ENSP00000379037.1:p.Asp386His
ENST00000395681.6:c.1156G>C (TYMP)	ENSP00000379038.1:p.Asp386His
ENST00000543927.6:c.-17G>C (SCO2)	ENSP00000444433.1:n.-17G>C
ENST00000651490.1:c.89G>C (TYMP)
ENST00000652401.1:c.657G>C (TYMP)
ENST00000252029.7:c.1156G>C (TYMP)	ENSP00000252029.3:p.Asp386His
ENST00000395678.7:c.1156G>C (TYMP)	ENSP00000379036.3:p.Asp386His
ENST00000395680.5:c.1156G>C (TYMP)	ENSP00000379037.1:p.Asp386His
ENST00000395681.5:c.1156G>C (TYMP)	ENSP00000379038.1:p.Asp386His
ENST00000423348.1:c.-17G>C	ENSP00000403570.1:n.-17G>C
ENST00000425169.1:c.1057G>C (TYMP)	ENSP00000395875.1:p.Asp353His
ENST00000476284.1:n.1162G>C (TYMP)
ENST00000487577.5:n.1443G>C (TYMP)
ENST00000543927.5:c.-17G>C	ENSP00000444433.1:n.-17G>C
NM_001113755.2:c.1156G>C (TYMP)	NP_001107227.1:p.Asp386His
NM_001113756.2:c.1156G>C (TYMP)	NP_001107228.1:p.Asp386His
NM_001169109.1:c.-17G>C (SCO2)	NP_001162580.1:n.-17G>C
NM_001257988.1:c.1156G>C , LRG_727t1:c.1156G>C (TYMP)	NP_001244917.1:p.Asp386His
NM_001257989.1:c.1156G>C , LRG_727t2:c.1156G>C (TYMP)	NP_001244918.1:p.Asp386His
NM_001953.4:c.1156G>C (TYMP)	NP_001944.1:p.Asp386His
NM_001113755.3:c.1156G>C (TYMP)	NP_001107227.1:p.Asp386His
NM_001113756.3:c.1156G>C (TYMP)	NP_001107228.1:p.Asp386His
NM_001953.5:c.1156G>C (TYMP) MANE Select	NP_001944.1:p.Asp386His
NM_001169109.2:c.-17G>C (SCO2)	NP_001162580.1:n.-17G>C