Canonical Allele Identifier: CA2263919582
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50197059G= , CM000679.2:g.50197059G= GRCh38
NC_000017.10:g.48274420G= , CM000679.1:g.48274420G= GRCh37
NC_000017.9:g.45629419G= NCBI36
NG_007400.1:g.9581C= , LRG_1:g.9581C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.755C= MANE Select ENSP00000225964.6:p.Ala252=
ENST00000225964.9:c.755C= ENSP00000225964.5:p.Ala252=
ENST00000495677.1:n.482C=
NM_000088.3:c.755C= , LRG_1t1:c.755C= NP_000079.2:p.Ala252=
XM_005257058.3:c.755C= XP_005257115.2:p.Ala252=
XM_005257059.3:c.755C= XP_005257116.2:p.Ala252=
XM_011524341.1:c.755C= XP_011522643.1:p.Ala252=
XM_005257058.4:c.755C= XP_005257115.2:p.Ala252=
XM_005257059.4:c.755C= XP_005257116.2:p.Ala252=
NM_000088.4:c.755C= MANE Select NP_000079.2:p.Ala252=