Canonical Allele Identifier: CA2263913828
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185748G= , CM000679.2:g.50185748G= GRCh38
NC_000017.10:g.48263109G= , CM000679.1:g.48263109G= GRCh37
NC_000017.9:g.45618108G= NCBI36
NG_007400.1:g.20892C= , LRG_1:g.20892C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4248+30C= MANE Select ENSP00000225964.6:n.4248+30C=
ENST00000225964.9:c.4248+30C= ENSP00000225964.5:n.4248+30C=
NM_000088.3:c.4248+30C= , LRG_1t1:c.4248+30C= NP_000079.2:n.4248+30C=
XM_005257058.3:c.3978+30C= XP_005257115.2:n.3978+30C=
XM_005257059.3:c.3330+30C= XP_005257116.2:n.3330+30C=
XM_011524341.1:c.4050+30C= XP_011522643.1:n.4050+30C=
XM_005257058.4:c.3978+30C= XP_005257115.2:n.3978+30C=
XM_005257059.4:c.3330+30C= XP_005257116.2:n.3330+30C=
NM_000088.4:c.4248+30C= MANE Select NP_000079.2:n.4248+30C=