Canonical Allele Identifier: CA1325080011

Gene: CPS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.210608379T= , CM000664.2:g.210608379T=	GRCh38
NC_000002.11:g.211473103T= , CM000664.1:g.211473103T=	GRCh37
NC_000002.10:g.211181348T=	NCBI36
NG_008285.1:g.135695T= , LRG_336:g.135695T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233072.10:c.2211T= MANE Select	ENSP00000233072.5:p.Ile737=
ENST00000430249.7:c.2229T=	ENSP00000402608.2:p.Ile743=
ENST00000451903.3:c.858T=	ENSP00000406136.2:p.Ile286=
ENST00000673510.1:c.2211T=	ENSP00000500537.1:p.Ile737=
ENST00000673630.1:c.2211T=	ENSP00000501073.1:p.Ile737=
ENST00000673698.1:c.691T=
ENST00000673711.1:c.2211T=	ENSP00000501022.1:p.Ile737=
ENST00000674074.1:n.1356T=
ENST00000233072.9:c.2211T=	ENSP00000233072.5:p.Ile737=
ENST00000430249.6:c.2229T=	ENSP00000402608.2:p.Ile743=
ENST00000451903.2:c.858T=	ENSP00000406136.2:p.Ile286=
NM_001122633.2:c.2229T=	NP_001116105.1:p.Ile743=
NM_001122634.3:c.858T=	NP_001116106.1:p.Ile286=
NM_001875.4:c.2211T= , LRG_336t1:c.2211T=	NP_001866.2:p.Ile737=
XM_011510640.1:c.2244T=	XP_011508942.1:p.Ile748=
XM_011510641.1:c.2211T=	XP_011508943.1:p.Ile737=
XM_011510642.1:c.2211T=	XP_011508944.1:p.Ile737=
XM_011510643.1:c.2211T=	XP_011508945.1:p.Ile737=
XM_011510644.1:c.2211T=	XP_011508946.1:p.Ile737=
NM_001122633.3:c.2211T=	NP_001116105.2:p.Ile737=
NM_001369256.1:c.2244T=	NP_001356185.1:p.Ile748=
NM_001369257.1:c.2211T=	NP_001356186.1:p.Ile737=
NM_001875.5:c.2211T= MANE Select	NP_001866.2:p.Ile737=
NR_161225.1:n.3120T=
NR_163592.1:n.1367T=