Canonical Allele Identifier: CA350440738

Gene: CPS1

Linked Data

• MyVariant Identifiers: chr2:g.211540506A>T (hg19) ; chr2:g.210675782A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.210675782A>T , CM000664.2:g.210675782A>T	GRCh38
NC_000002.11:g.211540506A>T , CM000664.1:g.211540506A>T	GRCh37
NC_000002.10:g.211248751A>T	NCBI36
NG_008285.1:g.203098A>T , LRG_336:g.203098A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233072.10:c.4216A>T MANE Select	ENSP00000233072.5:p.Thr1406Ser
ENST00000430249.7:c.4234A>T	ENSP00000402608.2:p.Thr1412Ser
ENST00000451903.3:c.2863A>T	ENSP00000406136.2:p.Thr955Ser
ENST00000645825.1:n.881A>T
ENST00000671984.1:n.364A>T
ENST00000673510.1:c.4216A>T	ENSP00000500537.1:p.Thr1406Ser
ENST00000673630.1:c.4216A>T	ENSP00000501073.1:p.Thr1406Ser
ENST00000673698.1:c.2839A>T
ENST00000673711.1:c.4216A>T	ENSP00000501022.1:p.Thr1406Ser
ENST00000674074.1:n.3361A>T
ENST00000233072.9:c.4216A>T	ENSP00000233072.5:p.Thr1406Ser
ENST00000430249.6:c.4234A>T	ENSP00000402608.2:p.Thr1412Ser
ENST00000451903.2:c.2863A>T	ENSP00000406136.2:p.Thr955Ser
ENST00000479988.1:n.3402A>T
NM_001122633.2:c.4234A>T	NP_001116105.1:p.Thr1412Ser
NM_001122634.3:c.2863A>T	NP_001116106.1:p.Thr955Ser
NM_001875.4:c.4216A>T , LRG_336t1:c.4216A>T	NP_001866.2:p.Thr1406Ser
XM_011510640.1:c.4249A>T	XP_011508942.1:p.Thr1417Ser
XM_011510641.1:c.4216A>T	XP_011508943.1:p.Thr1406Ser
XM_011510642.1:c.4216A>T	XP_011508944.1:p.Thr1406Ser
XM_011510643.1:c.4216A>T	XP_011508945.1:p.Thr1406Ser
XM_011510644.1:c.4216A>T	XP_011508946.1:p.Thr1406Ser
NM_001122633.3:c.4216A>T	NP_001116105.2:p.Thr1406Ser
NM_001369256.1:c.4249A>T	NP_001356185.1:p.Thr1417Ser
NM_001369257.1:c.4216A>T	NP_001356186.1:p.Thr1406Ser
NM_001875.5:c.4216A>T MANE Select	NP_001866.2:p.Thr1406Ser
NR_161225.1:n.5125A>T
NR_163592.1:n.3372A>T