Canonical Allele Identifier: CA1522596139

Gene: CLPTM1L

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1321972C= , CM000667.2:g.1321972C=	GRCh38
NC_000005.9:g.1322087C= , CM000667.1:g.1322087C=	GRCh37
NC_000005.8:g.1375087C=	NCBI36
NG_046903.1:g.28094G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320895.10:c.1316-153G= MANE Select	ENSP00000313854.5:n.1316-153G=
ENST00000320895.9:c.1316-153G=	ENSP00000313854.5:n.1316-153G=
ENST00000503042.5:n.2738-153G=
ENST00000503534.5:n.247-153G=
ENST00000505605.5:n.214-153G=
ENST00000505914.5:n.287-153G=
ENST00000506641.5:n.477-153G=
ENST00000507195.5:n.412-153G=
ENST00000507807.3:c.809-153G=	ENSP00000423321.1:n.809-153G=
ENST00000511268.6:n.80-153G=
ENST00000512451.5:n.40-153G=
ENST00000630539.1:c.809-153G=	ENSP00000485923.1:n.809-153G=
NM_030782.3:c.1316-153G=	NP_110409.2:n.1316-153G=
NM_030782.4:c.1316-153G=	NP_110409.2:n.1316-153G=
XM_011514144.1:c.1313-153G=	XP_011512446.1:n.1313-153G=
XM_011514144.2:c.1313-153G=	XP_011512446.1:n.1313-153G=
XM_024446221.1:c.1316-153G=	XP_024301989.1:n.1316-153G=
XM_024446222.1:c.782-153G=	XP_024301990.1:n.782-153G=
XR_002956182.1:n.1359-153G=
XR_002956183.1:n.1537-153G=
NM_030782.5:c.1316-153G= MANE Select	NP_110409.2:n.1316-153G=