Canonical Allele Identifier: CA2263913898
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185866G= , CM000679.2:g.50185866G= GRCh38
NC_000017.10:g.48263227G= , CM000679.1:g.48263227G= GRCh37
NC_000017.9:g.45618226G= NCBI36
NG_007400.1:g.20774C= , LRG_1:g.20774C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4160C= MANE Select ENSP00000225964.6:p.Ala1387=
ENST00000225964.9:c.4160C= ENSP00000225964.5:p.Ala1387=
ENST00000510710.3:n.1125C=
NM_000088.3:c.4160C= , LRG_1t1:c.4160C= NP_000079.2:p.Ala1387=
XM_005257058.3:c.3890C= XP_005257115.2:p.Ala1297=
XM_005257059.3:c.3242C= XP_005257116.2:p.Ala1081=
XM_011524341.1:c.3962C= XP_011522643.1:p.Ala1321=
XM_005257058.4:c.3890C= XP_005257115.2:p.Ala1297=
XM_005257059.4:c.3242C= XP_005257116.2:p.Ala1081=
NM_000088.4:c.4160C= MANE Select NP_000079.2:p.Ala1387=