Canonical Allele Identifier: CA2263913733
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185601G= , CM000679.2:g.50185601G= GRCh38
NC_000017.10:g.48262962G= , CM000679.1:g.48262962G= GRCh37
NC_000017.9:g.45617961G= NCBI36
NG_007400.1:g.21039C= , LRG_1:g.21039C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4296C= MANE Select ENSP00000225964.6:p.Thr1432=
ENST00000225964.9:c.4296C= ENSP00000225964.5:p.Thr1432=
NM_000088.3:c.4296C= , LRG_1t1:c.4296C= NP_000079.2:p.Thr1432=
XM_005257058.3:c.4026C= XP_005257115.2:p.Thr1342=
XM_005257059.3:c.3378C= XP_005257116.2:p.Thr1126=
XM_011524341.1:c.4098C= XP_011522643.1:p.Thr1366=
XM_005257058.4:c.4026C= XP_005257115.2:p.Thr1342=
XM_005257059.4:c.3378C= XP_005257116.2:p.Thr1126=
NM_000088.4:c.4296C= MANE Select NP_000079.2:p.Thr1432=