Canonical Allele Identifier: CA2263914950
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188056T= , CM000679.2:g.50188056T= GRCh38
NC_000017.10:g.48265417T= , CM000679.1:g.48265417T= GRCh37
NC_000017.9:g.45620416T= NCBI36
NG_007400.1:g.18584A= , LRG_1:g.18584A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.3261+40A= MANE Select ENSP00000225964.6:n.3261+40A=
ENST00000225964.9:c.3261+40A= ENSP00000225964.5:n.3261+40A=
ENST00000486572.1:n.459+40A=
ENST00000511732.1:n.625A=
NM_000088.3:c.3261+40A= , LRG_1t1:c.3261+40A= NP_000079.2:n.3261+40A=
XM_005257058.3:c.2991+40A= XP_005257115.2:n.2991+40A=
XM_005257059.3:c.2343+40A= XP_005257116.2:n.2343+40A=
XM_011524341.1:c.3063+40A= XP_011522643.1:n.3063+40A=
XM_005257058.4:c.2991+40A= XP_005257115.2:n.2991+40A=
XM_005257059.4:c.2343+40A= XP_005257116.2:n.2343+40A=
NM_000088.4:c.3261+40A= MANE Select NP_000079.2:n.3261+40A=