Canonical Allele Identifier: CA2263917616
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192825G= , CM000679.2:g.50192825G= GRCh38
NC_000017.10:g.48270186G= , CM000679.1:g.48270186G= GRCh37
NC_000017.9:g.45625185G= NCBI36
NG_007400.1:g.13815C= , LRG_1:g.13815C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1847C= MANE Select ENSP00000225964.6:p.Ala616=
ENST00000225964.9:c.1847C= ENSP00000225964.5:p.Ala616=
ENST00000476387.1:n.196C=
NM_000088.3:c.1847C= , LRG_1t1:c.1847C= NP_000079.2:p.Ala616=
XM_005257058.3:c.1847C= XP_005257115.2:p.Ala616=
XM_005257059.3:c.958-132C= XP_005257116.2:n.958-132C=
XM_011524341.1:c.1649C= XP_011522643.1:p.Ala550=
XM_005257058.4:c.1847C= XP_005257115.2:p.Ala616=
XM_005257059.4:c.958-132C= XP_005257116.2:n.958-132C=
NM_000088.4:c.1847C= MANE Select NP_000079.2:p.Ala616=