Canonical Allele Identifier: CA1621057436
Gene: CLPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35795160G= , CM000668.2:g.35795160G= GRCh38
NC_000006.11:g.35762937G= , CM000668.1:g.35762937G= GRCh37
NC_000006.10:g.35870915G= NCBI36
NG_012184.3:g.2955G=

Transcript Alleles

HGVS Amino-acid Change
NM_001832.4:c.325C= MANE Select NP_001823.1:p.Arg109=
ENST00000259938.7:c.325C= MANE Select ENSP00000259938.2:p.Arg109=
NM_001252597.1:c.283C= NP_001239526.1:p.Arg95=
NM_001252597.2:c.283C= NP_001239526.1:p.Arg95=
NM_001252598.1:c.202C= NP_001239527.1:p.Arg68=
NM_001252598.2:c.202C= NP_001239527.1:p.Arg68=
NM_001832.3:c.325C= NP_001823.1:p.Arg109=
ENST00000259938.6:c.325C= ENSP00000259938.2:p.Arg109=
ENST00000616014.3:c.202C= ENSP00000483589.1:p.Arg68=
ENST00000622413.2:c.283C= ENSP00000482919.1:p.Arg95=