Canonical Allele Identifier: CA2263918395
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194800C= , CM000679.2:g.50194800C= GRCh38
NC_000017.10:g.48272161C= , CM000679.1:g.48272161C= GRCh37
NC_000017.9:g.45627160C= NCBI36
NG_007400.1:g.11840G= , LRG_1:g.11840G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1382G= MANE Select ENSP00000225964.6:p.Gly461=
ENST00000225964.9:c.1382G= ENSP00000225964.5:p.Gly461=
ENST00000471344.1:n.326G=
NM_000088.3:c.1382G= , LRG_1t1:c.1382G= NP_000079.2:p.Gly461=
XM_005257058.3:c.1382G= XP_005257115.2:p.Gly461=
XM_005257059.3:c.957+1514G= XP_005257116.2:n.957+1514G=
XM_011524341.1:c.1184G= XP_011522643.1:p.Gly395=
XM_005257058.4:c.1382G= XP_005257115.2:p.Gly461=
XM_005257059.4:c.957+1514G= XP_005257116.2:n.957+1514G=
NM_000088.4:c.1382G= MANE Select NP_000079.2:p.Gly461=