Canonical Allele Identifier: CA2261633951

Gene: C1QL1 NMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44960751C= , CM000679.2:g.44960751C=	GRCh38
NC_000017.10:g.43038119C= , CM000679.1:g.43038119C=	GRCh37
NC_000017.9:g.40393645C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253407.4:c.598-384G= (C1QL1) MANE Select	ENSP00000253407.2:n.598-384G=
ENST00000678938.1:c.-110+2689C= (NMT1)	ENSP00000503621.1:n.-110+2689C=
ENST00000253407.3:c.598-384G= (C1QL1)	ENSP00000253407.2:n.598-384G=
NM_006688.4:c.598-384G= (C1QL1)	NP_006679.1:n.598-384G=
NM_006688.5:c.598-384G= (C1QL1) MANE Select	NP_006679.1:n.598-384G=