Canonical Allele Identifier: CA2263917611
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192819G= , CM000679.2:g.50192819G= GRCh38
NC_000017.10:g.48270180G= , CM000679.1:g.48270180G= GRCh37
NC_000017.9:g.45625179G= NCBI36
NG_007400.1:g.13821C= , LRG_1:g.13821C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1853C= MANE Select ENSP00000225964.6:p.Ala618=
ENST00000225964.9:c.1853C= ENSP00000225964.5:p.Ala618=
ENST00000476387.1:n.202C=
NM_000088.3:c.1853C= , LRG_1t1:c.1853C= NP_000079.2:p.Ala618=
XM_005257058.3:c.1853C= XP_005257115.2:p.Ala618=
XM_005257059.3:c.958-126C= XP_005257116.2:n.958-126C=
XM_011524341.1:c.1655C= XP_011522643.1:p.Ala552=
XM_005257058.4:c.1853C= XP_005257115.2:p.Ala618=
XM_005257059.4:c.958-126C= XP_005257116.2:n.958-126C=
NM_000088.4:c.1853C= MANE Select NP_000079.2:p.Ala618=