Canonical Allele Identifier: CA2263913890
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185855G= , CM000679.2:g.50185855G= GRCh38
NC_000017.10:g.48263216G= , CM000679.1:g.48263216G= GRCh37
NC_000017.9:g.45618215G= NCBI36
NG_007400.1:g.20785C= , LRG_1:g.20785C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4171C= MANE Select ENSP00000225964.6:p.Gln1391=
ENST00000225964.9:c.4171C= ENSP00000225964.5:p.Gln1391=
ENST00000510710.3:n.1136C=
NM_000088.3:c.4171C= , LRG_1t1:c.4171C= NP_000079.2:p.Gln1391=
XM_005257058.3:c.3901C= XP_005257115.2:p.Gln1301=
XM_005257059.3:c.3253C= XP_005257116.2:p.Gln1085=
XM_011524341.1:c.3973C= XP_011522643.1:p.Gln1325=
XM_005257058.4:c.3901C= XP_005257115.2:p.Gln1301=
XM_005257059.4:c.3253C= XP_005257116.2:p.Gln1085=
NM_000088.4:c.4171C= MANE Select NP_000079.2:p.Gln1391=