Canonical Allele Identifier: CA10098788

Gene: CLTCL1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19234536G>A , CM000684.2:g.19234536G>A	GRCh38
NC_000022.10:g.19222059G>A , CM000684.1:g.19222059G>A	GRCh37
NC_000022.9:g.17602059G>A	NCBI36
NG_033805.1:g.62181C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427926.6:c.1140C>T MANE Select	ENSP00000441158.1:p.Ala380=
ENST00000427926.5:c.1140C>T	ENSP00000441158.1:p.Ala380=
ENST00000615606.4:n.1160C>T
ENST00000617103.4:c.1140C>T	ENSP00000480709.1:p.Ala380=
ENST00000621271.4:c.1140C>T	ENSP00000485020.1:p.Ala380=
NM_001835.3:c.1140C>T	NP_001826.3:p.Ala380=
NM_007098.3:c.1140C>T	NP_009029.3:p.Ala380=
XM_005277800.2:c.1203C>T	XP_005277857.1:p.Ala401=
XM_005277801.2:c.1203C>T	XP_005277858.1:p.Ala401=
XM_006724328.1:c.1203C>T	XP_006724391.1:p.Ala401=
XM_011530395.1:c.1203C>T	XP_011528697.1:p.Ala401=
XM_011530396.1:c.1089C>T	XP_011528698.1:p.Ala363=
XM_011530397.1:c.1203C>T	XP_011528699.1:p.Ala401=
XM_011530398.1:c.1203C>T	XP_011528700.1:p.Ala401=
XM_011530399.1:c.1203C>T	XP_011528701.1:p.Ala401=
XM_011530400.1:c.1203C>T	XP_011528702.1:p.Ala401=
XR_937923.1:n.1208C>T
XR_937924.1:n.1286C>T
XM_017028953.2:c.1140C>T	XP_016884442.1:p.Ala380=
XM_017028954.2:c.1026C>T	XP_016884443.1:p.Ala342=
XM_017028955.2:c.1140C>T	XP_016884444.1:p.Ala380=
XM_017028956.2:c.1140C>T	XP_016884445.1:p.Ala380=
XM_017028957.2:c.1140C>T	XP_016884446.1:p.Ala380=
XR_001755309.2:n.1213C>T
XR_001755310.2:n.1213C>T
XR_001755311.2:n.1213C>T
XR_001755312.2:n.1213C>T
XR_001755313.2:n.1213C>T
XR_001755314.2:n.1213C>T
XR_937923.3:n.1213C>T
NM_007098.4:c.1140C>T MANE Select	NP_009029.3:p.Ala380=
NM_001835.4:c.1140C>T	NP_001826.3:p.Ala380=