Canonical Allele Identifier: CA2395768548

Gene: CLTCL1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19196584T= , CM000684.2:g.19196584T=	GRCh38
NC_000022.10:g.19184095T= , CM000684.1:g.19184095T=	GRCh37
NC_000022.9:g.17564095T=	NCBI36
NG_033805.1:g.100133A=

Transcript Alleles

HGVS	Amino-acid Change
NM_007098.4:c.3946A= MANE Select	NP_009029.3:p.Met1316=
ENST00000427926.6:c.3946A= MANE Select	ENSP00000441158.1:p.Met1316=
NM_001835.3:c.3946A=	NP_001826.3:p.Met1316=
NM_001835.4:c.3946A=	NP_001826.3:p.Met1316=
NM_007098.3:c.3946A=	NP_009029.3:p.Met1316=
ENST00000427926.5:c.3946A=	ENSP00000441158.1:p.Met1316=
ENST00000611723.1:n.690A=
ENST00000615606.4:n.3966A=
ENST00000617103.4:c.*101A=	ENSP00000480709.1:n.*101A=
ENST00000617926.4:c.415A=	ENSP00000481031.1:p.Met139=
ENST00000621271.4:c.3946A=	ENSP00000485020.1:p.Met1316=
ENST00000622493.4:c.415A=	ENSP00000479237.1:p.Met139=
XM_005277800.2:c.4009A=	XP_005277857.1:p.Met1337=
XM_005277801.2:c.4009A=	XP_005277858.1:p.Met1337=
XM_006724328.1:c.4009A=	XP_006724391.1:p.Met1337=
XM_011530395.1:c.4009A=	XP_011528697.1:p.Met1337=
XM_011530396.1:c.3895A=	XP_011528698.1:p.Met1299=
XM_011530397.1:c.3736A=	XP_011528699.1:p.Met1246=
XM_011530398.1:c.4009A=	XP_011528700.1:p.Met1337=
XM_011530399.1:c.*101A=	XP_011528701.1:n.*101A=
XM_011530401.1:c.2137A=	XP_011528703.1:p.Met713=
XM_011530401.2:c.2137A=	XP_011528703.1:p.Met713=
XM_017028953.2:c.3946A=	XP_016884442.1:p.Met1316=
XM_017028954.2:c.3832A=	XP_016884443.1:p.Met1278=
XM_017028955.2:c.3730A=	XP_016884444.1:p.Met1244=
XM_017028956.2:c.3946A=	XP_016884445.1:p.Met1316=
XR_001755309.2:n.4019A=
XR_001755310.2:n.3957A=
XR_001755311.2:n.3865A=
XR_001755312.2:n.3865A=
XR_001755313.2:n.3861A=
XR_001755314.2:n.3861A=
XR_002958736.1:n.186T=
XR_937923.1:n.3952A=
XR_937923.3:n.3957A=
XR_937924.1:n.3934A=