Canonical Allele Identifier: CA400227440
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199294G>T , CM000679.2:g.50199294G>T GRCh38
NC_000017.10:g.48276655G>T , CM000679.1:g.48276655G>T GRCh37
NC_000017.9:g.45631654G>T NCBI36
NG_007400.1:g.7346C>A , LRG_1:g.7346C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.403C>A MANE Select ENSP00000225964.6:p.Pro135Thr
ENST00000225964.9:c.403C>A ENSP00000225964.5:p.Pro135Thr
ENST00000474644.1:n.624C>A
ENST00000507689.1:c.457C>A ENSP00000460459.1:p.Pro153Thr
NM_000088.3:c.403C>A , LRG_1t1:c.403C>A NP_000079.2:p.Pro135Thr
XM_005257058.3:c.403C>A XP_005257115.2:p.Pro135Thr
XM_005257059.3:c.403C>A XP_005257116.2:p.Pro135Thr
XM_011524341.1:c.403C>A XP_011522643.1:p.Pro135Thr
XM_005257058.4:c.403C>A XP_005257115.2:p.Pro135Thr
XM_005257059.4:c.403C>A XP_005257116.2:p.Pro135Thr
NM_000088.4:c.403C>A MANE Select NP_000079.2:p.Pro135Thr