Canonical Allele Identifier: CA10099018

Gene: CLTCL1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19254165C>T , CM000684.2:g.19254165C>T	GRCh38
NC_000022.10:g.19241688C>T , CM000684.1:g.19241688C>T	GRCh37
NC_000022.9:g.17621688C>T	NCBI36
NG_033805.1:g.42552G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427926.6:c.313G>A MANE Select	ENSP00000441158.1:p.Ala105Thr
ENST00000427926.5:c.313G>A	ENSP00000441158.1:p.Ala105Thr
ENST00000449918.1:c.376G>A	ENSP00000443264.1:p.Ala126Thr
ENST00000615606.4:n.333G>A
ENST00000617103.4:c.313G>A	ENSP00000480709.1:p.Ala105Thr
ENST00000621271.4:c.313G>A	ENSP00000485020.1:p.Ala105Thr
NM_001835.3:c.313G>A	NP_001826.3:p.Ala105Thr
NM_007098.3:c.313G>A	NP_009029.3:p.Ala105Thr
XM_005277800.2:c.376G>A	XP_005277857.1:p.Ala126Thr
XM_005277801.2:c.376G>A	XP_005277858.1:p.Ala126Thr
XM_006724328.1:c.376G>A	XP_006724391.1:p.Ala126Thr
XM_011530395.1:c.376G>A	XP_011528697.1:p.Ala126Thr
XM_011530396.1:c.376G>A	XP_011528698.1:p.Ala126Thr
XM_011530397.1:c.376G>A	XP_011528699.1:p.Ala126Thr
XM_011530398.1:c.376G>A	XP_011528700.1:p.Ala126Thr
XM_011530399.1:c.376G>A	XP_011528701.1:p.Ala126Thr
XM_011530400.1:c.376G>A	XP_011528702.1:p.Ala126Thr
XR_937923.1:n.381G>A
XR_937924.1:n.459G>A
XM_017028953.2:c.313G>A	XP_016884442.1:p.Ala105Thr
XM_017028954.2:c.313G>A	XP_016884443.1:p.Ala105Thr
XM_017028955.2:c.313G>A	XP_016884444.1:p.Ala105Thr
XM_017028956.2:c.313G>A	XP_016884445.1:p.Ala105Thr
XM_017028957.2:c.313G>A	XP_016884446.1:p.Ala105Thr
XR_001755309.2:n.386G>A
XR_001755310.2:n.386G>A
XR_001755311.2:n.386G>A
XR_001755312.2:n.386G>A
XR_001755313.2:n.386G>A
XR_001755314.2:n.386G>A
XR_937923.3:n.386G>A
NM_007098.4:c.313G>A MANE Select	NP_009029.3:p.Ala105Thr
NM_001835.4:c.313G>A	NP_001826.3:p.Ala105Thr