Canonical Allele Identifier: CA1522583302
Gene: CLPTM1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1342599C= , CM000667.2:g.1342599C= GRCh38
NC_000005.9:g.1342714C= , CM000667.1:g.1342714C= GRCh37
NC_000005.8:g.1395714C= NCBI36
NG_046903.1:g.7467G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320895.10:c.264-739G= MANE Select ENSP00000313854.5:n.264-739G=
ENST00000320895.9:c.264-739G= ENSP00000313854.5:n.264-739G=
ENST00000630539.1:c.-136-739G= ENSP00000485923.1:n.-136-739G=
NM_030782.3:c.264-739G= NP_110409.2:n.264-739G=
NM_030782.4:c.264-739G= NP_110409.2:n.264-739G=
XM_011514144.1:c.264-739G= XP_011512446.1:n.264-739G=
XM_011514144.2:c.264-739G= XP_011512446.1:n.264-739G=
XM_024446221.1:c.264-739G= XP_024301989.1:n.264-739G=
XR_002956182.1:n.307-739G=
XR_002956183.1:n.488-739G=
NM_030782.5:c.264-739G= MANE Select NP_110409.2:n.264-739G=