Canonical Allele Identifier: CA1729841513

Gene: COL26A1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.101472713C= , CM000669.2:g.101472713C=	GRCh38
NC_000007.13:g.101115994C= , CM000669.1:g.101115994C=	GRCh37
NC_000007.12:g.100902714C=	NCBI36
NG_033785.2:g.114894C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001278563.3:c.385+24926C= MANE Select	NP_001265492.1:n.385+24926C=
ENST00000313669.12:c.385+24926C= MANE Select	ENSP00000318234.8:n.385+24926C=
NM_001278563.2:c.385+24926C=	NP_001265492.1:n.385+24926C=
NM_133457.4:c.379+24926C=	NP_597714.2:n.379+24926C=
NM_133457.5:c.379+24926C=	NP_597714.2:n.379+24926C=
ENST00000313669.11:c.385+24926C=	ENSP00000318234.8:n.385+24926C=
ENST00000613501.1:c.379+24926C=	ENSP00000482102.1:n.379+24926C=
XM_017011743.1:c.385+24926C=	XP_016867232.1:n.385+24926C=
XM_017011744.1:c.-6+24926C=	XP_016867233.1:n.-6+24926C=
XM_017011745.1:c.-6+24926C=	XP_016867234.1:n.-6+24926C=