Canonical Allele Identifier: CA2263914998
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188132G= , CM000679.2:g.50188132G= GRCh38
NC_000017.10:g.48265493G= , CM000679.1:g.48265493G= GRCh37
NC_000017.9:g.45620492G= NCBI36
NG_007400.1:g.18508C= , LRG_1:g.18508C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.3225C= MANE Select ENSP00000225964.6:p.Ala1075=
ENST00000225964.9:c.3225C= ENSP00000225964.5:p.Ala1075=
ENST00000486572.1:n.423C=
ENST00000511732.1:n.549C=
NM_000088.3:c.3225C= , LRG_1t1:c.3225C= NP_000079.2:p.Ala1075=
XM_005257058.3:c.2955C= XP_005257115.2:p.Ala985=
XM_005257059.3:c.2307C= XP_005257116.2:p.Ala769=
XM_011524341.1:c.3027C= XP_011522643.1:p.Ala1009=
XM_005257058.4:c.2955C= XP_005257115.2:p.Ala985=
XM_005257059.4:c.2307C= XP_005257116.2:p.Ala769=
NM_000088.4:c.3225C= MANE Select NP_000079.2:p.Ala1075=