Canonical Allele Identifier: CA10097639

Gene: CLTCL1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19183443C>T , CM000684.2:g.19183443C>T	GRCh38
NC_000022.10:g.19170956C>T , CM000684.1:g.19170956C>T	GRCh37
NC_000022.9:g.17550956C>T	NCBI36
NG_033805.1:g.113274G>A
NG_033863.1:g.421G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427926.6:c.4774G>A MANE Select	ENSP00000441158.1:p.Val1592Met
ENST00000412649.5:n.1389G>A
ENST00000427926.5:c.4774G>A	ENSP00000441158.1:p.Val1592Met
ENST00000615606.4:n.4867G>A
ENST00000617103.4:c.*929G>A	ENSP00000480709.1:n.*929G>A
ENST00000617926.4:c.1243G>A	ENSP00000481031.1:p.Val415Met
ENST00000621271.4:c.4603G>A	ENSP00000485020.1:p.Val1535Met
ENST00000622493.4:c.961G>A	ENSP00000479237.1:p.Val321Met
NM_001835.3:c.4603G>A	NP_001826.3:p.Val1535Met
NM_007098.3:c.4774G>A	NP_009029.3:p.Val1592Met
XM_005277800.2:c.4837G>A	XP_005277857.1:p.Val1613Met
XM_005277801.2:c.4666G>A	XP_005277858.1:p.Val1556Met
XM_006724328.1:c.4555G>A	XP_006724391.1:p.Val1519Met
XM_011530395.1:c.4837G>A	XP_011528697.1:p.Val1613Met
XM_011530396.1:c.4723G>A	XP_011528698.1:p.Val1575Met
XM_011530397.1:c.4564G>A	XP_011528699.1:p.Val1522Met
XM_011530401.1:c.2965G>A	XP_011528703.1:p.Val989Met
XR_937924.1:n.4480G>A
XM_011530401.2:c.2965G>A	XP_011528703.1:p.Val989Met
XM_017028953.2:c.4774G>A	XP_016884442.1:p.Val1592Met
XM_017028954.2:c.4660G>A	XP_016884443.1:p.Val1554Met
XM_017028955.2:c.4558G>A	XP_016884444.1:p.Val1520Met
XM_017028956.2:c.4492G>A	XP_016884445.1:p.Val1498Met
XR_001755309.2:n.4981G>A
XR_001755310.2:n.4785G>A
XR_001755311.2:n.4522G>A
XR_001755312.2:n.4411G>A
XR_001755313.2:n.4518G>A
XR_001755314.2:n.4407G>A
XR_937923.3:n.4614G>A
NM_007098.4:c.4774G>A MANE Select	NP_009029.3:p.Val1592Met
NM_001835.4:c.4603G>A	NP_001826.3:p.Val1535Met