Canonical Allele Identifier: CA2263917241
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50193000G= , CM000679.2:g.50193000G= GRCh38
NC_000017.10:g.48270361G= , CM000679.1:g.48270361G= GRCh37
NC_000017.9:g.45625360G= NCBI36
NG_007400.1:g.13640C= , LRG_1:g.13640C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1815C= MANE Select ENSP00000225964.6:p.Gly605=
ENST00000225964.9:c.1815C= ENSP00000225964.5:p.Gly605=
ENST00000476387.1:n.164C=
NM_000088.3:c.1815C= , LRG_1t1:c.1815C= NP_000079.2:p.Gly605=
XM_005257058.3:c.1815C= XP_005257115.2:p.Gly605=
XM_005257059.3:c.958-307C= XP_005257116.2:n.958-307C=
XM_011524341.1:c.1617C= XP_011522643.1:p.Gly539=
XM_005257058.4:c.1815C= XP_005257115.2:p.Gly605=
XM_005257059.4:c.958-307C= XP_005257116.2:n.958-307C=
NM_000088.4:c.1815C= MANE Select NP_000079.2:p.Gly605=