Canonical Allele Identifier: CA2263913910
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185890T= , CM000679.2:g.50185890T= GRCh38
NC_000017.10:g.48263251T= , CM000679.1:g.48263251T= GRCh37
NC_000017.9:g.45618250T= NCBI36
NG_007400.1:g.20750A= , LRG_1:g.20750A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4136A= MANE Select ENSP00000225964.6:p.Gln1379=
ENST00000225964.9:c.4136A= ENSP00000225964.5:p.Gln1379=
ENST00000510710.3:n.1101A=
NM_000088.3:c.4136A= , LRG_1t1:c.4136A= NP_000079.2:p.Gln1379=
XM_005257058.3:c.3866A= XP_005257115.2:p.Gln1289=
XM_005257059.3:c.3218A= XP_005257116.2:p.Gln1073=
XM_011524341.1:c.3938A= XP_011522643.1:p.Gln1313=
XM_005257058.4:c.3866A= XP_005257115.2:p.Gln1289=
XM_005257059.4:c.3218A= XP_005257116.2:p.Gln1073=
NM_000088.4:c.4136A= MANE Select NP_000079.2:p.Gln1379=