Canonical Allele Identifier: CA2263918022
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194117G= , CM000679.2:g.50194117G= GRCh38
NC_000017.10:g.48271478G= , CM000679.1:g.48271478G= GRCh37
NC_000017.9:g.45626477G= NCBI36
NG_007400.1:g.12523C= , LRG_1:g.12523C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1668+13C= MANE Select ENSP00000225964.6:n.1668+13C=
ENST00000225964.9:c.1668+13C= ENSP00000225964.5:n.1668+13C=
ENST00000463440.1:n.58+13C=
ENST00000471344.1:n.625C=
NM_000088.3:c.1668+13C= , LRG_1t1:c.1668+13C= NP_000079.2:n.1668+13C=
XM_005257058.3:c.1668+13C= XP_005257115.2:n.1668+13C=
XM_005257059.3:c.958-1424C= XP_005257116.2:n.958-1424C=
XM_011524341.1:c.1470+13C= XP_011522643.1:n.1470+13C=
XM_005257058.4:c.1668+13C= XP_005257115.2:n.1668+13C=
XM_005257059.4:c.958-1424C= XP_005257116.2:n.958-1424C=
NM_000088.4:c.1668+13C= MANE Select NP_000079.2:n.1668+13C=