Canonical Allele Identifier: CA10321473

Gene: TYMP SCO2

Linked Data

• ClinVar Variation Id: 223065
• ClinVar RCV Id: RCV000208672 ; RCV000794156
• dbSNP Id: rs770277446
• ExAC: 22:50964673 A / T
• gnomAD v2: 22-50964673-A-T
• gnomAD v4: 22-50526244-A-T
• MyVariant Identifiers: chr22:g.50964673A>T (hg19) ; chr22:g.50526244A>T (hg38)
• PubMed: PMID:12529715 ; PMID:20301358

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50526244A>T , CM000684.2:g.50526244A>T	GRCh38
NC_000022.10:g.50964673A>T , CM000684.1:g.50964673A>T	GRCh37
NC_000022.9:g.49311539A>T	NCBI36
NG_011860.1:g.8842T>A , LRG_727:g.8842T>A
NG_016235.1:g.5196T>A
NG_021419.1:g.23029A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000252029.8:c.1159+2T>A (TYMP) MANE Select	ENSP00000252029.3:n.1159+2T>A
ENST00000395680.6:c.1159+2T>A (TYMP)	ENSP00000379037.1:n.1159+2T>A
ENST00000395681.6:c.1159+2T>A (TYMP)	ENSP00000379038.1:n.1159+2T>A
ENST00000543927.6:c.-14+2T>A (SCO2)	ENSP00000444433.1:n.-14+2T>A
ENST00000651490.1:c.92+2T>A (TYMP)
ENST00000652401.1:c.660+2T>A (TYMP)
ENST00000252029.7:c.1159+2T>A (TYMP)	ENSP00000252029.3:n.1159+2T>A
ENST00000395678.7:c.1159+2T>A (TYMP)	ENSP00000379036.3:n.1159+2T>A
ENST00000395680.5:c.1159+2T>A (TYMP)	ENSP00000379037.1:n.1159+2T>A
ENST00000395681.5:c.1159+2T>A (TYMP)	ENSP00000379038.1:n.1159+2T>A
ENST00000423348.1:c.-14+2T>A	ENSP00000403570.1:n.-14+2T>A
ENST00000425169.1:c.1060+2T>A (TYMP)	ENSP00000395875.1:n.1060+2T>A
ENST00000476284.1:n.1167T>A (TYMP)
ENST00000487577.5:n.1446+2T>A (TYMP)
ENST00000543927.5:c.-14+2T>A	ENSP00000444433.1:n.-14+2T>A
NM_001113755.2:c.1159+2T>A (TYMP)	NP_001107227.1:n.1159+2T>A
NM_001113756.2:c.1159+2T>A (TYMP)	NP_001107228.1:n.1159+2T>A
NM_001169109.1:c.-14+2T>A (SCO2)	NP_001162580.1:n.-14+2T>A
NM_001257988.1:c.1159+2T>A , LRG_727t1:c.1159+2T>A (TYMP)	NP_001244917.1:n.1159+2T>A
NM_001257989.1:c.1159+2T>A , LRG_727t2:c.1159+2T>A (TYMP)	NP_001244918.1:n.1159+2T>A
NM_001953.4:c.1159+2T>A (TYMP)	NP_001944.1:n.1159+2T>A
NM_001113755.3:c.1159+2T>A (TYMP)	NP_001107227.1:n.1159+2T>A
NM_001113756.3:c.1159+2T>A (TYMP)	NP_001107228.1:n.1159+2T>A
NM_001953.5:c.1159+2T>A (TYMP) MANE Select	NP_001944.1:n.1159+2T>A
NM_001169109.2:c.-14+2T>A (SCO2)	NP_001162580.1:n.-14+2T>A