Canonical Allele Identifier: CA287528841

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8227671G>A , CM000679.2:g.8227671G>A	GRCh38
NC_000017.10:g.8130989G>A , CM000679.1:g.8130989G>A	GRCh37
NC_000017.9:g.8071714G>A	NCBI36
NG_032148.1:g.25425C>T
NG_032148.2:g.25425C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025099.6:c.*509C>T MANE Select	NP_079375.3:n.*509C>T
ENST00000651323.1:c.*509C>T MANE Select	ENSP00000498499.1:n.*509C>T
NM_025099.5:c.*509C>T	NP_079375.3:n.*509C>T
NR_046431.1:n.4052C>T
NR_046431.2:n.4013C>T
ENST00000315684.12:c.*509C>T	ENSP00000313759.8:n.*509C>T
ENST00000449476.6:c.*897C>T	ENSP00000396018.2:n.*897C>T
ENST00000449476.7:c.*897C>T	ENSP00000396018.2:n.*897C>T
ENST00000643543.1:c.*2870C>T	ENSP00000494323.1:n.*2870C>T
ENST00000699849.1:c.*509C>T	ENSP00000514647.1:n.*509C>T
ENST00000699850.1:n.4095C>T
ENST00000699851.1:n.5049C>T
ENST00000699852.1:c.*2676C>T	ENSP00000514648.1:n.*2676C>T
ENST00000699853.1:c.*748C>T	ENSP00000514649.1:n.*748C>T
XM_006721577.2:c.*509C>T	XP_006721640.1:n.*509C>T
XM_006721577.3:c.*509C>T	XP_006721640.1:n.*509C>T
XM_006721578.2:c.*509C>T	XP_006721641.1:n.*509C>T
XM_006721578.3:c.*509C>T	XP_006721641.1:n.*509C>T
XM_011524010.1:c.*509C>T	XP_011522312.1:n.*509C>T
XM_011524010.2:c.*509C>T	XP_011522312.1:n.*509C>T
XM_011524011.1:c.*509C>T	XP_011522313.1:n.*509C>T
XM_011524011.2:c.*509C>T	XP_011522313.1:n.*509C>T
XR_001752639.1:n.4014C>T
XR_001752640.1:n.4162C>T
XR_001752641.1:n.4097C>T
XR_001752642.1:n.3947C>T
XR_002958073.1:n.4453C>T
XR_429823.2:n.4040C>T
XR_429823.3:n.4040C>T
XR_429824.2:n.4141C>T
XR_429824.3:n.4141C>T