Canonical Allele Identifier: CA1685998120
Gene: COL28A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.7359708T= , CM000669.2:g.7359708T= GRCh38
NC_000007.13:g.7399339T= , CM000669.1:g.7399339T= GRCh37
NC_000007.12:g.7365864T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000399429.8:c.3205+682A= MANE Select ENSP00000382356.3:n.3205+682A=
ENST00000399429.7:c.3205+682A= ENSP00000382356.3:n.3205+682A=
ENST00000430711.5:c.256+682A= ENSP00000413093.1:n.256+682A=
ENST00000453441.1:c.70+682A= ENSP00000391380.1:n.70+682A=
NM_001037763.2:c.3205+682A= NP_001032852.2:n.3205+682A=
XM_011515358.1:c.3205+682A= XP_011513660.1:n.3205+682A=
XM_011515359.1:c.3205+682A= XP_011513661.1:n.3205+682A=
XM_011515360.1:c.3205+682A= XP_011513662.1:n.3205+682A=
XM_011515362.1:c.2056+682A= XP_011513664.1:n.2056+682A=
XR_926936.1:n.3408+682A=
XM_011515358.3:c.3205+682A= XP_011513660.1:n.3205+682A=
XM_011515359.2:c.3205+682A= XP_011513661.1:n.3205+682A=
XM_011515360.2:c.3205+682A= XP_011513662.1:n.3205+682A=
XM_011515362.2:c.2056+682A= XP_011513664.1:n.2056+682A=
XM_017012131.2:c.3205+682A= XP_016867620.1:n.3205+682A=
XM_017012132.2:c.3205+682A= XP_016867621.1:n.3205+682A=
XR_001744688.1:n.4831+682A=
XR_926936.3:n.4607+682A=
NM_001037763.3:c.3205+682A= MANE Select NP_001032852.2:n.3205+682A=