Canonical Allele Identifier: CA2263917612
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192820C= , CM000679.2:g.50192820C= GRCh38
NC_000017.10:g.48270181C= , CM000679.1:g.48270181C= GRCh37
NC_000017.9:g.45625180C= NCBI36
NG_007400.1:g.13820G= , LRG_1:g.13820G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1852G= MANE Select ENSP00000225964.6:p.Ala618=
ENST00000225964.9:c.1852G= ENSP00000225964.5:p.Ala618=
ENST00000476387.1:n.201G=
NM_000088.3:c.1852G= , LRG_1t1:c.1852G= NP_000079.2:p.Ala618=
XM_005257058.3:c.1852G= XP_005257115.2:p.Ala618=
XM_005257059.3:c.958-127G= XP_005257116.2:n.958-127G=
XM_011524341.1:c.1654G= XP_011522643.1:p.Ala552=
XM_005257058.4:c.1852G= XP_005257115.2:p.Ala618=
XM_005257059.4:c.958-127G= XP_005257116.2:n.958-127G=
NM_000088.4:c.1852G= MANE Select NP_000079.2:p.Ala618=