Canonical Allele Identifier: CA2263918012
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194109T= , CM000679.2:g.50194109T= GRCh38
NC_000017.10:g.48271470T= , CM000679.1:g.48271470T= GRCh37
NC_000017.9:g.45626469T= NCBI36
NG_007400.1:g.12531A= , LRG_1:g.12531A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1668+21A= MANE Select ENSP00000225964.6:n.1668+21A=
ENST00000225964.9:c.1668+21A= ENSP00000225964.5:n.1668+21A=
ENST00000463440.1:n.58+21A=
ENST00000471344.1:n.633A=
NM_000088.3:c.1668+21A= , LRG_1t1:c.1668+21A= NP_000079.2:n.1668+21A=
XM_005257058.3:c.1668+21A= XP_005257115.2:n.1668+21A=
XM_005257059.3:c.958-1416A= XP_005257116.2:n.958-1416A=
XM_011524341.1:c.1470+21A= XP_011522643.1:n.1470+21A=
XM_005257058.4:c.1668+21A= XP_005257115.2:n.1668+21A=
XM_005257059.4:c.958-1416A= XP_005257116.2:n.958-1416A=
NM_000088.4:c.1668+21A= MANE Select NP_000079.2:n.1668+21A=