Canonical Allele Identifier: CA8371771

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8228577G>C , CM000679.2:g.8228577G>C	GRCh38
NC_000017.10:g.8131895G>C , CM000679.1:g.8131895G>C	GRCh37
NC_000017.9:g.8072620G>C	NCBI36
NG_032148.1:g.24519C>G
NG_032148.2:g.24519C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000580299.2:c.3176C>G	ENSP00000462607.2:p.Thr1059Ser
ENST00000581729.2:c.3209C>G	ENSP00000462720.2:p.Thr1070Ser
ENST00000699849.1:c.2312C>G	ENSP00000514647.1:p.Thr771Ser
ENST00000699850.1:n.3372C>G
ENST00000699851.1:n.4326C>G
ENST00000699852.1:c.*1953C>G	ENSP00000514648.1:n.*1953C>G
ENST00000699853.1:c.*25C>G	ENSP00000514649.1:n.*25C>G
ENST00000699854.1:n.3999C>G
ENST00000699855.1:n.4563C>G
ENST00000699856.1:c.*391C>G	ENSP00000514650.1:n.*391C>G
ENST00000699857.1:n.4019C>G
ENST00000699858.1:c.*2724C>G	ENSP00000514651.1:n.*2724C>G
ENST00000699859.1:c.*176C>G	ENSP00000514652.1:n.*176C>G
ENST00000699860.1:n.2118C>G
ENST00000699861.1:n.3903C>G
ENST00000449476.7:c.*174C>G	ENSP00000396018.2:n.*174C>G
ENST00000581671.2:n.3429C>G
ENST00000643543.1:c.*2147C>G	ENSP00000494323.1:n.*2147C>G
ENST00000651323.1:c.3440C>G MANE Select	ENSP00000498499.1:p.Thr1147Ser
ENST00000315684.12:c.3440C>G	ENSP00000313759.8:p.Thr1147Ser
ENST00000449476.6:c.*174C>G	ENSP00000396018.2:n.*174C>G
ENST00000580299.1:c.347C>G	ENSP00000462607.1:p.Thr116Ser
ENST00000581729.1:c.157C>G
NM_025099.5:c.3440C>G	NP_079375.3:p.Thr1147Ser
NR_046431.1:n.3329C>G
XM_006721577.2:c.3311C>G	XP_006721640.1:p.Thr1104Ser
XM_006721578.2:c.3209C>G	XP_006721641.1:p.Thr1070Ser
XM_011524010.1:c.3335C>G	XP_011522312.1:p.Thr1112Ser
XM_011524011.1:c.2543C>G	XP_011522313.1:p.Thr848Ser
XR_429823.2:n.3317C>G
XR_429824.2:n.3418C>G
NM_025099.6:c.3440C>G MANE Select	NP_079375.3:p.Thr1147Ser
XM_006721577.3:c.3311C>G	XP_006721640.1:p.Thr1104Ser
XM_006721578.3:c.3209C>G	XP_006721641.1:p.Thr1070Ser
XM_011524010.2:c.3335C>G	XP_011522312.1:p.Thr1112Ser
XM_011524011.2:c.2543C>G	XP_011522313.1:p.Thr848Ser
XR_001752639.1:n.3291C>G
XR_001752640.1:n.3439C>G
XR_001752641.1:n.3374C>G
XR_001752642.1:n.3224C>G
XR_002958073.1:n.3730C>G
XR_429823.3:n.3317C>G
XR_429824.3:n.3418C>G
NR_046431.2:n.3290C>G