Canonical Allele Identifier: CA539123601

Gene: CPS1

Linked Data

• dbSNP Id: rs1383540502
• gnomAD v2: 2-211504675-A-G
• gnomAD v4: 2-210639951-A-G
• MyVariant Identifiers: chr2:g.211504675A>G (hg19) ; chr2:g.210639951A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.210639951A>G , CM000664.2:g.210639951A>G	GRCh38
NC_000002.11:g.211504675A>G , CM000664.1:g.211504675A>G	GRCh37
NC_000002.10:g.211212920A>G	NCBI36
NG_008285.1:g.167267A>G , LRG_336:g.167267A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000233072.10:c.2896-45A>G MANE Select	ENSP00000233072.5:n.2896-45A>G
ENST00000430249.7:c.2914-45A>G	ENSP00000402608.2:n.2914-45A>G
ENST00000451903.3:c.1543-45A>G	ENSP00000406136.2:n.1543-45A>G
ENST00000673510.1:c.2896-45A>G	ENSP00000500537.1:n.2896-45A>G
ENST00000673630.1:c.2896-45A>G	ENSP00000501073.1:n.2896-45A>G
ENST00000673698.1:c.1376-45A>G
ENST00000673711.1:c.2896-45A>G	ENSP00000501022.1:n.2896-45A>G
ENST00000674074.1:n.2041-45A>G
ENST00000233072.9:c.2896-45A>G	ENSP00000233072.5:n.2896-45A>G
ENST00000430249.6:c.2914-45A>G	ENSP00000402608.2:n.2914-45A>G
ENST00000451903.2:c.1543-45A>G	ENSP00000406136.2:n.1543-45A>G
ENST00000497121.1:n.268-45A>G
NM_001122633.2:c.2914-45A>G	NP_001116105.1:n.2914-45A>G
NM_001122634.3:c.1543-45A>G	NP_001116106.1:n.1543-45A>G
NM_001875.4:c.2896-45A>G , LRG_336t1:c.2896-45A>G	NP_001866.2:n.2896-45A>G
XM_011510640.1:c.2929-45A>G	XP_011508942.1:n.2929-45A>G
XM_011510641.1:c.2896-45A>G	XP_011508943.1:n.2896-45A>G
XM_011510642.1:c.2896-45A>G	XP_011508944.1:n.2896-45A>G
XM_011510643.1:c.2896-45A>G	XP_011508945.1:n.2896-45A>G
XM_011510644.1:c.2896-45A>G	XP_011508946.1:n.2896-45A>G
NM_001122633.3:c.2896-45A>G	NP_001116105.2:n.2896-45A>G
NM_001369256.1:c.2929-45A>G	NP_001356185.1:n.2929-45A>G
NM_001369257.1:c.2896-45A>G	NP_001356186.1:n.2896-45A>G
NM_001875.5:c.2896-45A>G MANE Select	NP_001866.2:n.2896-45A>G
NR_161225.1:n.3805-45A>G
NR_163592.1:n.2052-45A>G