Canonical Allele Identifier: CA2263918352
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194727G= , CM000679.2:g.50194727G= GRCh38
NC_000017.10:g.48272088G= , CM000679.1:g.48272088G= GRCh37
NC_000017.9:g.45627087G= NCBI36
NG_007400.1:g.11913C= , LRG_1:g.11913C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1455C= MANE Select ENSP00000225964.6:p.Gly485=
ENST00000225964.9:c.1455C= ENSP00000225964.5:p.Gly485=
ENST00000471344.1:n.399C=
NM_000088.3:c.1455C= , LRG_1t1:c.1455C= NP_000079.2:p.Gly485=
XM_005257058.3:c.1455C= XP_005257115.2:p.Gly485=
XM_005257059.3:c.957+1587C= XP_005257116.2:n.957+1587C=
XM_011524341.1:c.1257C= XP_011522643.1:p.Gly419=
XM_005257058.4:c.1455C= XP_005257115.2:p.Gly485=
XM_005257059.4:c.957+1587C= XP_005257116.2:n.957+1587C=
NM_000088.4:c.1455C= MANE Select NP_000079.2:p.Gly485=