Canonical Allele Identifier: CA2263919345
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196620A= , CM000679.2:g.50196620A= GRCh38
NC_000017.10:g.48273981A= , CM000679.1:g.48273981A= GRCh37
NC_000017.9:g.45628980A= NCBI36
NG_007400.1:g.10020T= , LRG_1:g.10020T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.855T= MANE Select ENSP00000225964.6:p.Pro285=
ENST00000225964.9:c.855T= ENSP00000225964.5:p.Pro285=
ENST00000495677.1:n.582T=
NM_000088.3:c.855T= , LRG_1t1:c.855T= NP_000079.2:p.Pro285=
XM_005257058.3:c.855T= XP_005257115.2:p.Pro285=
XM_005257059.3:c.855T= XP_005257116.2:p.Pro285=
XM_011524341.1:c.855T= XP_011522643.1:p.Pro285=
XM_005257058.4:c.855T= XP_005257115.2:p.Pro285=
XM_005257059.4:c.855T= XP_005257116.2:p.Pro285=
NM_000088.4:c.855T= MANE Select NP_000079.2:p.Pro285=