Canonical Allele Identifier: CA2263913908
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185886C= , CM000679.2:g.50185886C= GRCh38
NC_000017.10:g.48263247C= , CM000679.1:g.48263247C= GRCh37
NC_000017.9:g.45618246C= NCBI36
NG_007400.1:g.20754G= , LRG_1:g.20754G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4140G= MANE Select ENSP00000225964.6:p.Gln1380=
ENST00000225964.9:c.4140G= ENSP00000225964.5:p.Gln1380=
ENST00000510710.3:n.1105G=
NM_000088.3:c.4140G= , LRG_1t1:c.4140G= NP_000079.2:p.Gln1380=
XM_005257058.3:c.3870G= XP_005257115.2:p.Gln1290=
XM_005257059.3:c.3222G= XP_005257116.2:p.Gln1074=
XM_011524341.1:c.3942G= XP_011522643.1:p.Gln1314=
XM_005257058.4:c.3870G= XP_005257115.2:p.Gln1290=
XM_005257059.4:c.3222G= XP_005257116.2:p.Gln1074=
NM_000088.4:c.4140G= MANE Select NP_000079.2:p.Gln1380=