Canonical Allele Identifier: CA2263919307
Community Standard Title: NM_000088.4(COL1A1):c.859-14T=
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196542A= , CM000679.2:g.50196542A= GRCh38
NC_000017.10:g.48273903A= , CM000679.1:g.48273903A= GRCh37
NC_000017.9:g.45628902A= NCBI36
NG_007400.1:g.10098T= , LRG_1:g.10098T=

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.859-14T= MANE Select NP_000079.2:n.859-14T=
ENST00000225964.10:c.859-14T= MANE Select ENSP00000225964.6:n.859-14T=
NM_000088.3:c.859-14T= , LRG_1t1:c.859-14T= NP_000079.2:n.859-14T=
ENST00000225964.9:c.859-14T= ENSP00000225964.5:n.859-14T=
ENST00000485870.1:n.54T=
ENST00000495677.1:n.586-14T=
XM_005257058.3:c.859-14T= XP_005257115.2:n.859-14T=
XM_005257058.4:c.859-14T= XP_005257115.2:n.859-14T=
XM_005257059.3:c.859-14T= XP_005257116.2:n.859-14T=
XM_005257059.4:c.859-14T= XP_005257116.2:n.859-14T=
XM_011524341.1:c.859-14T= XP_011522643.1:n.859-14T=