Canonical Allele Identifier: CA2263916148
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50190323T= , CM000679.2:g.50190323T= GRCh38
NC_000017.10:g.48267684T= , CM000679.1:g.48267684T= GRCh37
NC_000017.9:g.45622683T= NCBI36
NG_007400.1:g.16317A= , LRG_1:g.16317A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.2451+4A= MANE Select ENSP00000225964.6:n.2451+4A=
ENST00000225964.9:c.2451+4A= ENSP00000225964.5:n.2451+4A=
ENST00000494334.1:n.382A=
NM_000088.3:c.2451+4A= , LRG_1t1:c.2451+4A= NP_000079.2:n.2451+4A=
XM_005257058.3:c.2451+4A= XP_005257115.2:n.2451+4A=
XM_005257059.3:c.1533+4A= XP_005257116.2:n.1533+4A=
XM_011524341.1:c.2253+4A= XP_011522643.1:n.2253+4A=
XM_005257058.4:c.2451+4A= XP_005257115.2:n.2451+4A=
XM_005257059.4:c.1533+4A= XP_005257116.2:n.1533+4A=
NM_000088.4:c.2451+4A= MANE Select NP_000079.2:n.2451+4A=