Canonical Allele Identifier: CA2263918386
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194780T= , CM000679.2:g.50194780T= GRCh38
NC_000017.10:g.48272141T= , CM000679.1:g.48272141T= GRCh37
NC_000017.9:g.45627140T= NCBI36
NG_007400.1:g.11860A= , LRG_1:g.11860A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1402A= MANE Select ENSP00000225964.6:p.Lys468=
ENST00000225964.9:c.1402A= ENSP00000225964.5:p.Lys468=
ENST00000471344.1:n.346A=
NM_000088.3:c.1402A= , LRG_1t1:c.1402A= NP_000079.2:p.Lys468=
XM_005257058.3:c.1402A= XP_005257115.2:p.Lys468=
XM_005257059.3:c.957+1534A= XP_005257116.2:n.957+1534A=
XM_011524341.1:c.1204A= XP_011522643.1:p.Lys402=
XM_005257058.4:c.1402A= XP_005257115.2:p.Lys468=
XM_005257059.4:c.957+1534A= XP_005257116.2:n.957+1534A=
NM_000088.4:c.1402A= MANE Select NP_000079.2:p.Lys468=