Canonical Allele Identifier: CA2263919130
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196202G= , CM000679.2:g.50196202G= GRCh38
NC_000017.10:g.48273563G= , CM000679.1:g.48273563G= GRCh37
NC_000017.9:g.45628562G= NCBI36
NG_007400.1:g.10438C= , LRG_1:g.10438C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.958-3C= MANE Select ENSP00000225964.6:n.958-3C=
ENST00000225964.9:c.958-3C= ENSP00000225964.5:n.958-3C=
ENST00000485870.1:n.283-3C=
NM_000088.3:c.958-3C= , LRG_1t1:c.958-3C= NP_000079.2:n.958-3C=
XM_005257058.3:c.958-3C= XP_005257115.2:n.958-3C=
XM_005257059.3:c.957+112C= XP_005257116.2:n.957+112C=
XM_011524341.1:c.957+112C= XP_011522643.1:n.957+112C=
XM_005257058.4:c.958-3C= XP_005257115.2:n.958-3C=
XM_005257059.4:c.957+112C= XP_005257116.2:n.957+112C=
NM_000088.4:c.958-3C= MANE Select NP_000079.2:n.958-3C=