Canonical Allele Identifier: CA400189749
Gene: COL1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185502T>G , CM000679.2:g.50185502T>G GRCh38
NC_000017.10:g.48262863T>G , CM000679.1:g.48262863T>G GRCh37
NC_000017.9:g.45617862T>G NCBI36
NG_007400.1:g.21138A>C , LRG_1:g.21138A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4395A>C MANE Select ENSP00000225964.6:p.Ter1465Tyr
ENST00000225964.9:c.4395A>C ENSP00000225964.5:p.Ter1465Tyr
NM_000088.3:c.4395A>C , LRG_1t1:c.4395A>C NP_000079.2:p.Ter1465Tyr
XM_005257058.3:c.4125A>C XP_005257115.2:p.Ter1375Tyr
XM_005257059.3:c.3477A>C XP_005257116.2:p.Ter1159Tyr
XM_011524341.1:c.4197A>C XP_011522643.1:p.Ter1399Tyr
XM_005257058.4:c.4125A>C XP_005257115.2:p.Ter1375Tyr
XM_005257059.4:c.3477A>C XP_005257116.2:p.Ter1159Tyr
NM_000088.4:c.4395A>C MANE Select NP_000079.2:p.Ter1465Tyr