Canonical Allele Identifier: CA2838484695

Gene: CPS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.210675659A>C , CM000664.2:g.210675659A>C	GRCh38
NC_000002.11:g.211540383A>C , CM000664.1:g.211540383A>C	GRCh37
NC_000002.10:g.211248628A>C	NCBI36
NG_008285.1:g.202975A>C , LRG_336:g.202975A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233072.10:c.4162-69A>C MANE Select	ENSP00000233072.5:n.4162-69A>C
ENST00000430249.7:c.4180-69A>C	ENSP00000402608.2:n.4180-69A>C
ENST00000451903.3:c.2809-69A>C	ENSP00000406136.2:n.2809-69A>C
ENST00000645825.1:n.827-69A>C
ENST00000671984.1:n.310-69A>C
ENST00000673510.1:c.4162-69A>C	ENSP00000500537.1:n.4162-69A>C
ENST00000673630.1:c.4162-69A>C	ENSP00000501073.1:n.4162-69A>C
ENST00000673698.1:c.2785-69A>C
ENST00000673711.1:c.4162-69A>C	ENSP00000501022.1:n.4162-69A>C
ENST00000674074.1:n.3307-69A>C
ENST00000233072.9:c.4162-69A>C	ENSP00000233072.5:n.4162-69A>C
ENST00000430249.6:c.4180-69A>C	ENSP00000402608.2:n.4180-69A>C
ENST00000451903.2:c.2809-69A>C	ENSP00000406136.2:n.2809-69A>C
ENST00000479988.1:n.3348-69A>C
NM_001122633.2:c.4180-69A>C	NP_001116105.1:n.4180-69A>C
NM_001122634.3:c.2809-69A>C	NP_001116106.1:n.2809-69A>C
NM_001875.4:c.4162-69A>C , LRG_336t1:c.4162-69A>C	NP_001866.2:n.4162-69A>C
XM_011510640.1:c.4195-69A>C	XP_011508942.1:n.4195-69A>C
XM_011510641.1:c.4162-69A>C	XP_011508943.1:n.4162-69A>C
XM_011510642.1:c.4162-69A>C	XP_011508944.1:n.4162-69A>C
XM_011510643.1:c.4162-69A>C	XP_011508945.1:n.4162-69A>C
XM_011510644.1:c.4162-69A>C	XP_011508946.1:n.4162-69A>C
NM_001122633.3:c.4162-69A>C	NP_001116105.2:n.4162-69A>C
NM_001369256.1:c.4195-69A>C	NP_001356185.1:n.4195-69A>C
NM_001369257.1:c.4162-69A>C	NP_001356186.1:n.4162-69A>C
NM_001875.5:c.4162-69A>C MANE Select	NP_001866.2:n.4162-69A>C
NR_161225.1:n.5071-69A>C
NR_163592.1:n.3318-69A>C