Canonical Allele Identifier: CA2263914949
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188055G= , CM000679.2:g.50188055G= GRCh38
NC_000017.10:g.48265416G= , CM000679.1:g.48265416G= GRCh37
NC_000017.9:g.45620415G= NCBI36
NG_007400.1:g.18585C= , LRG_1:g.18585C=

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.3261+41C= MANE Select ENSP00000225964.6:n.3261+41C=
ENST00000225964.9:c.3261+41C= ENSP00000225964.5:n.3261+41C=
ENST00000486572.1:n.459+41C=
ENST00000511732.1:n.626C=
NM_000088.3:c.3261+41C= , LRG_1t1:c.3261+41C= NP_000079.2:n.3261+41C=
XM_005257058.3:c.2991+41C= XP_005257115.2:n.2991+41C=
XM_005257059.3:c.2343+41C= XP_005257116.2:n.2343+41C=
XM_011524341.1:c.3063+41C= XP_011522643.1:n.3063+41C=
XM_005257058.4:c.2991+41C= XP_005257115.2:n.2991+41C=
XM_005257059.4:c.2343+41C= XP_005257116.2:n.2343+41C=
NM_000088.4:c.3261+41C= MANE Select NP_000079.2:n.3261+41C=