Canonical Allele Identifier: CA2086602

Gene: CPS1

Linked Data

• dbSNP Id: rs750831111
• ExAC: 2:211473194 T / C
• gnomAD v2: 2-211473194-T-C
• gnomAD v4: 2-210608470-T-C
• MyVariant Identifiers: chr2:g.211473194T>C (hg19) ; chr2:g.210608470T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.210608470T>C , CM000664.2:g.210608470T>C	GRCh38
NC_000002.11:g.211473194T>C , CM000664.1:g.211473194T>C	GRCh37
NC_000002.10:g.211181439T>C	NCBI36
NG_008285.1:g.135786T>C , LRG_336:g.135786T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233072.10:c.2302T>C MANE Select	ENSP00000233072.5:p.Tyr768His
ENST00000430249.7:c.2320T>C	ENSP00000402608.2:p.Tyr774His
ENST00000451903.3:c.949T>C	ENSP00000406136.2:p.Tyr317His
ENST00000673510.1:c.2302T>C	ENSP00000500537.1:p.Tyr768His
ENST00000673630.1:c.2302T>C	ENSP00000501073.1:p.Tyr768His
ENST00000673698.1:c.782T>C
ENST00000673711.1:c.2302T>C	ENSP00000501022.1:p.Tyr768His
ENST00000674074.1:n.1447T>C
ENST00000233072.9:c.2302T>C	ENSP00000233072.5:p.Tyr768His
ENST00000430249.6:c.2320T>C	ENSP00000402608.2:p.Tyr774His
ENST00000451903.2:c.949T>C	ENSP00000406136.2:p.Tyr317His
NM_001122633.2:c.2320T>C	NP_001116105.1:p.Tyr774His
NM_001122634.3:c.949T>C	NP_001116106.1:p.Tyr317His
NM_001875.4:c.2302T>C , LRG_336t1:c.2302T>C	NP_001866.2:p.Tyr768His
XM_011510640.1:c.2335T>C	XP_011508942.1:p.Tyr779His
XM_011510641.1:c.2302T>C	XP_011508943.1:p.Tyr768His
XM_011510642.1:c.2302T>C	XP_011508944.1:p.Tyr768His
XM_011510643.1:c.2302T>C	XP_011508945.1:p.Tyr768His
XM_011510644.1:c.2302T>C	XP_011508946.1:p.Tyr768His
NM_001122633.3:c.2302T>C	NP_001116105.2:p.Tyr768His
NM_001369256.1:c.2335T>C	NP_001356185.1:p.Tyr779His
NM_001369257.1:c.2302T>C	NP_001356186.1:p.Tyr768His
NM_001875.5:c.2302T>C MANE Select	NP_001866.2:p.Tyr768His
NR_161225.1:n.3211T>C
NR_163592.1:n.1458T>C