Canonical Allele Identifier: CA2263917488
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192673A= , CM000679.2:g.50192673A= GRCh38
NC_000017.10:g.48270034A= , CM000679.1:g.48270034A= GRCh37
NC_000017.9:g.45625033A= NCBI36
NG_007400.1:g.13967T= , LRG_1:g.13967T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1896T= MANE Select ENSP00000225964.6:p.Gly632=
ENST00000225964.9:c.1896T= ENSP00000225964.5:p.Gly632=
ENST00000476387.1:n.245T=
NM_000088.3:c.1896T= , LRG_1t1:c.1896T= NP_000079.2:p.Gly632=
XM_005257058.3:c.1896T= XP_005257115.2:p.Gly632=
XM_005257059.3:c.978T= XP_005257116.2:p.Gly326=
XM_011524341.1:c.1698T= XP_011522643.1:p.Gly566=
XM_005257058.4:c.1896T= XP_005257115.2:p.Gly632=
XM_005257059.4:c.978T= XP_005257116.2:p.Gly326=
NM_000088.4:c.1896T= MANE Select NP_000079.2:p.Gly632=