Canonical Allele Identifier: CA2395761963

Gene: CLTCL1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_007098.4:c.4774G= MANE Select	NP_009029.3:p.Val1592=
ENST00000427926.6:c.4774G= MANE Select	ENSP00000441158.1:p.Val1592=
NM_001835.3:c.4603G=	NP_001826.3:p.Val1535=
NM_001835.4:c.4603G=	NP_001826.3:p.Val1535=
NM_007098.3:c.4774G=	NP_009029.3:p.Val1592=
ENST00000412649.5:n.1389G=
ENST00000427926.5:c.4774G=	ENSP00000441158.1:p.Val1592=
ENST00000615606.4:n.4867G=
ENST00000617103.4:c.*929G=	ENSP00000480709.1:n.*929G=
ENST00000617926.4:c.1243G=	ENSP00000481031.1:p.Val415=
ENST00000621271.4:c.4603G=	ENSP00000485020.1:p.Val1535=
ENST00000622493.4:c.961G=	ENSP00000479237.1:p.Val321=
XM_005277800.2:c.4837G=	XP_005277857.1:p.Val1613=
XM_005277801.2:c.4666G=	XP_005277858.1:p.Val1556=
XM_006724328.1:c.4555G=	XP_006724391.1:p.Val1519=
XM_011530395.1:c.4837G=	XP_011528697.1:p.Val1613=
XM_011530396.1:c.4723G=	XP_011528698.1:p.Val1575=
XM_011530397.1:c.4564G=	XP_011528699.1:p.Val1522=
XM_011530401.1:c.2965G=	XP_011528703.1:p.Val989=
XM_011530401.2:c.2965G=	XP_011528703.1:p.Val989=
XM_017028953.2:c.4774G=	XP_016884442.1:p.Val1592=
XM_017028954.2:c.4660G=	XP_016884443.1:p.Val1554=
XM_017028955.2:c.4558G=	XP_016884444.1:p.Val1520=
XM_017028956.2:c.4492G=	XP_016884445.1:p.Val1498=
XR_001755309.2:n.4981G=
XR_001755310.2:n.4785G=
XR_001755311.2:n.4522G=
XR_001755312.2:n.4411G=
XR_001755313.2:n.4518G=
XR_001755314.2:n.4407G=
XR_937923.3:n.4614G=
XR_937924.1:n.4480G=