Canonical Allele Identifier: CA1685998111

Gene: COL28A1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.7359705G= , CM000669.2:g.7359705G=	GRCh38
NC_000007.13:g.7399336G= , CM000669.1:g.7399336G=	GRCh37
NC_000007.12:g.7365861G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399429.8:c.3205+685C= MANE Select	ENSP00000382356.3:n.3205+685C=
ENST00000399429.7:c.3205+685C=	ENSP00000382356.3:n.3205+685C=
ENST00000430711.5:c.256+685C=	ENSP00000413093.1:n.256+685C=
ENST00000453441.1:c.70+685C=	ENSP00000391380.1:n.70+685C=
NM_001037763.2:c.3205+685C=	NP_001032852.2:n.3205+685C=
XM_011515358.1:c.3205+685C=	XP_011513660.1:n.3205+685C=
XM_011515359.1:c.3205+685C=	XP_011513661.1:n.3205+685C=
XM_011515360.1:c.3205+685C=	XP_011513662.1:n.3205+685C=
XM_011515362.1:c.2056+685C=	XP_011513664.1:n.2056+685C=
XR_926936.1:n.3408+685C=
XM_011515358.3:c.3205+685C=	XP_011513660.1:n.3205+685C=
XM_011515359.2:c.3205+685C=	XP_011513661.1:n.3205+685C=
XM_011515360.2:c.3205+685C=	XP_011513662.1:n.3205+685C=
XM_011515362.2:c.2056+685C=	XP_011513664.1:n.2056+685C=
XM_017012131.2:c.3205+685C=	XP_016867620.1:n.3205+685C=
XM_017012132.2:c.3205+685C=	XP_016867621.1:n.3205+685C=
XR_001744688.1:n.4831+685C=
XR_926936.3:n.4607+685C=
NM_001037763.3:c.3205+685C= MANE Select	NP_001032852.2:n.3205+685C=