Canonical Allele Identifier: CA3774248

Gene: CLPS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35797166T>C , CM000668.2:g.35797166T>C	GRCh38
NC_000006.11:g.35764943T>C , CM000668.1:g.35764943T>C	GRCh37
NC_000006.10:g.35872921T>C	NCBI36
NG_012184.3:g.4961T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001832.4:c.84+39A>G MANE Select	NP_001823.1:n.84+39A>G
ENST00000259938.7:c.84+39A>G MANE Select	ENSP00000259938.2:n.84+39A>G
NM_001252597.1:c.-57+39A>G	NP_001239526.1:n.-57+39A>G
NM_001252597.2:c.-57+39A>G	NP_001239526.1:n.-57+39A>G
NM_001252598.1:c.84+39A>G	NP_001239527.1:n.84+39A>G
NM_001252598.2:c.84+39A>G	NP_001239527.1:n.84+39A>G
NM_001832.3:c.84+39A>G	NP_001823.1:n.84+39A>G
ENST00000259938.6:c.84+39A>G	ENSP00000259938.2:n.84+39A>G
ENST00000616014.3:c.84+39A>G	ENSP00000483589.1:n.84+39A>G