Canonical Allele Identifier: CA2581292483

Gene: CTC1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8227549A>G , CM000679.2:g.8227549A>G	GRCh38
NC_000017.10:g.8130867A>G , CM000679.1:g.8130867A>G	GRCh37
NC_000017.9:g.8071592A>G	NCBI36
NG_032148.1:g.25547T>C
NG_032148.2:g.25547T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025099.6:c.*631T>C MANE Select	NP_079375.3:n.*631T>C
ENST00000651323.1:c.*631T>C MANE Select	ENSP00000498499.1:n.*631T>C
NM_025099.5:c.*631T>C	NP_079375.3:n.*631T>C
NR_046431.1:n.4174T>C
NR_046431.2:n.4135T>C
ENST00000315684.12:c.*631T>C	ENSP00000313759.8:n.*631T>C
ENST00000449476.6:c.*1019T>C	ENSP00000396018.2:n.*1019T>C
ENST00000449476.7:c.*1019T>C	ENSP00000396018.2:n.*1019T>C
ENST00000643543.1:c.*2992T>C	ENSP00000494323.1:n.*2992T>C
ENST00000699849.1:c.*631T>C	ENSP00000514647.1:n.*631T>C
ENST00000699850.1:n.4217T>C
ENST00000699851.1:n.5171T>C
ENST00000699852.1:c.*2798T>C	ENSP00000514648.1:n.*2798T>C
ENST00000699853.1:c.*870T>C	ENSP00000514649.1:n.*870T>C
XM_006721577.2:c.*631T>C	XP_006721640.1:n.*631T>C
XM_006721577.3:c.*631T>C	XP_006721640.1:n.*631T>C
XM_006721578.2:c.*631T>C	XP_006721641.1:n.*631T>C
XM_006721578.3:c.*631T>C	XP_006721641.1:n.*631T>C
XM_011524010.1:c.*631T>C	XP_011522312.1:n.*631T>C
XM_011524010.2:c.*631T>C	XP_011522312.1:n.*631T>C
XM_011524011.1:c.*631T>C	XP_011522313.1:n.*631T>C
XM_011524011.2:c.*631T>C	XP_011522313.1:n.*631T>C
XR_001752639.1:n.4136T>C
XR_001752640.1:n.4284T>C
XR_001752641.1:n.4219T>C
XR_001752642.1:n.4069T>C
XR_002958073.1:n.4575T>C
XR_429823.2:n.4162T>C
XR_429823.3:n.4162T>C
XR_429824.2:n.4263T>C
XR_429824.3:n.4263T>C