Canonical Allele Identifier: CA795207

Gene: CTPS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40985007C>T , CM000663.2:g.40985007C>T	GRCh38
NC_000001.10:g.41450679C>T , CM000663.1:g.41450679C>T	GRCh37
NC_000001.9:g.41223266C>T	NCBI36
NG_034208.1:g.10709C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001905.4:c.337+16C>T MANE Select	NP_001896.2:n.337+16C>T
ENST00000650070.2:c.337+16C>T MANE Select	ENSP00000497602.1:n.337+16C>T
NM_001905.3:c.337+16C>T	NP_001896.2:n.337+16C>T
NR_125440.1:n.881+16C>T
NR_125440.2:n.484+16C>T
ENST00000372616.1:c.337+16C>T	ENSP00000361699.1:n.337+16C>T
ENST00000372621.8:c.337+16C>T	ENSP00000361704.4:n.337+16C>T
ENST00000463285.6:c.337+16C>T	ENSP00000497762.1:n.337+16C>T
ENST00000463285.7:c.337+16C>T	ENSP00000497762.1:n.337+16C>T
ENST00000470271.6:c.337+16C>T	ENSP00000497901.2:n.337+16C>T
ENST00000479480.5:n.418+16C>T
ENST00000479480.6:n.418+16C>T
ENST00000480420.6:n.492+16C>T
ENST00000498694.2:n.439+16C>T
ENST00000648020.1:c.337+16C>T	ENSP00000497714.1:n.337+16C>T
ENST00000648020.2:c.337+16C>T	ENSP00000497714.1:n.337+16C>T
ENST00000648801.1:n.423+16C>T
ENST00000648914.1:c.337+16C>T	ENSP00000496963.1:n.337+16C>T
ENST00000649124.1:c.337+16C>T	ENSP00000497744.1:n.337+16C>T
ENST00000649124.2:c.337+16C>T	ENSP00000497744.1:n.337+16C>T
ENST00000649864.1:c.337+16C>T	ENSP00000496792.1:n.337+16C>T
ENST00000650634.1:n.341+16C>T
ENST00000650634.2:n.474+16C>T
ENST00000696070.1:c.-139+5178C>T	ENSP00000512372.1:n.-139+5178C>T
ENST00000696107.1:c.337+16C>T	ENSP00000512401.1:n.337+16C>T
ENST00000696108.1:c.337+16C>T	ENSP00000512402.1:n.337+16C>T
ENST00000696109.1:n.699+16C>T
XM_005270536.1:c.337+16C>T	XP_005270593.1:n.337+16C>T
XM_006710390.2:c.337+16C>T	XP_006710453.1:n.337+16C>T
XM_006710391.1:c.337+16C>T	XP_006710454.1:n.337+16C>T
XM_011540821.1:c.358+16C>T	XP_011539123.1:n.358+16C>T
XM_011540822.1:c.358+16C>T	XP_011539124.1:n.358+16C>T
XM_024453552.1:c.358+16C>T	XP_024309320.1:n.358+16C>T
XM_024453553.1:c.337+16C>T	XP_024309321.1:n.337+16C>T
XM_024453554.1:c.337+16C>T	XP_024309322.1:n.337+16C>T
XM_024453561.1:c.358+16C>T	XP_024309329.1:n.358+16C>T
XR_001737003.1:n.484+16C>T
XR_001737004.1:n.484+16C>T
XR_002959539.1:n.482+16C>T
XR_946557.1:n.487+16C>T