Canonical Allele Identifier: CA339903842
Community Standard Title: NM_001905.4(CTPS1):c.720+1G>A
Gene: CTPS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40991846G>A , CM000663.2:g.40991846G>A GRCh38
NC_000001.10:g.41457518G>A , CM000663.1:g.41457518G>A GRCh37
NC_000001.9:g.41230105G>A NCBI36
NG_034208.1:g.17548G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001905.4:c.720+1G>A MANE Select NP_001896.2:n.720+1G>A
ENST00000650070.2:c.720+1G>A MANE Select ENSP00000497602.1:n.720+1G>A
NM_001301237.1:c.252+1G>A NP_001288166.1:n.252+1G>A
NM_001301237.2:c.252+1G>A NP_001288166.1:n.252+1G>A
NM_001905.3:c.720+1G>A NP_001896.2:n.720+1G>A
NR_125440.1:n.1264+1G>A
NR_125440.2:n.867+1G>A
ENST00000372616.1:c.720+1G>A ENSP00000361699.1:n.720+1G>A
ENST00000372621.8:c.720+1G>A ENSP00000361704.4:n.720+1G>A
ENST00000463285.6:c.720+1G>A ENSP00000497762.1:n.720+1G>A
ENST00000463285.7:c.720+1G>A ENSP00000497762.1:n.720+1G>A
ENST00000470271.6:c.720+1G>A ENSP00000497901.2:n.720+1G>A
ENST00000479480.6:n.801+1G>A
ENST00000480420.5:n.379+1G>A
ENST00000480420.6:n.875+1G>A
ENST00000498694.2:n.822+1G>A
ENST00000648020.1:c.720+1G>A ENSP00000497714.1:n.720+1G>A
ENST00000648020.2:c.720+1G>A ENSP00000497714.1:n.720+1G>A
ENST00000648801.1:n.806+1G>A
ENST00000648914.1:c.720+1G>A ENSP00000496963.1:n.720+1G>A
ENST00000649124.1:c.720+1G>A ENSP00000497744.1:n.720+1G>A
ENST00000649124.2:c.720+1G>A ENSP00000497744.1:n.720+1G>A
ENST00000649215.1:c.252+1G>A ENSP00000497698.1:n.252+1G>A
ENST00000649864.1:c.720+1G>A ENSP00000496792.1:n.720+1G>A
ENST00000650634.1:n.724+1G>A
ENST00000650634.2:n.857+1G>A
ENST00000696070.1:c.27+1G>A ENSP00000512372.1:n.27+1G>A
ENST00000696107.1:c.720+1G>A ENSP00000512401.1:n.720+1G>A
ENST00000696108.1:c.720+1G>A ENSP00000512402.1:n.720+1G>A
ENST00000696109.1:n.1082+1G>A
XM_005270536.1:c.720+1G>A XP_005270593.1:n.720+1G>A
XM_006710390.2:c.720+1G>A XP_006710453.1:n.720+1G>A
XM_006710391.1:c.720+1G>A XP_006710454.1:n.720+1G>A
XM_011540821.1:c.741+1G>A XP_011539123.1:n.741+1G>A
XM_011540822.1:c.741+1G>A XP_011539124.1:n.741+1G>A
XM_024453552.1:c.741+1G>A XP_024309320.1:n.741+1G>A
XM_024453553.1:c.720+1G>A XP_024309321.1:n.720+1G>A
XM_024453554.1:c.720+1G>A XP_024309322.1:n.720+1G>A
XM_024453561.1:c.741+1G>A XP_024309329.1:n.741+1G>A
XR_001737003.1:n.867+1G>A
XR_001737004.1:n.867+1G>A
XR_002959539.1:n.865+1G>A
XR_946557.1:n.870+1G>A