Canonical Allele Identifier: CA2263918370
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194750T= , CM000679.2:g.50194750T= GRCh38
NC_000017.10:g.48272111T= , CM000679.1:g.48272111T= GRCh37
NC_000017.9:g.45627110T= NCBI36
NG_007400.1:g.11890A= , LRG_1:g.11890A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1432A= MANE Select ENSP00000225964.6:p.Thr478=
ENST00000225964.9:c.1432A= ENSP00000225964.5:p.Thr478=
ENST00000471344.1:n.376A=
NM_000088.3:c.1432A= , LRG_1t1:c.1432A= NP_000079.2:p.Thr478=
XM_005257058.3:c.1432A= XP_005257115.2:p.Thr478=
XM_005257059.3:c.957+1564A= XP_005257116.2:n.957+1564A=
XM_011524341.1:c.1234A= XP_011522643.1:p.Thr412=
XM_005257058.4:c.1432A= XP_005257115.2:p.Thr478=
XM_005257059.4:c.957+1564A= XP_005257116.2:n.957+1564A=
NM_000088.4:c.1432A= MANE Select NP_000079.2:p.Thr478=