Canonical Allele Identifier: CA2263918325
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194688G= , CM000679.2:g.50194688G= GRCh38
NC_000017.10:g.48272049G= , CM000679.1:g.48272049G= GRCh37
NC_000017.9:g.45627048G= NCBI36
NG_007400.1:g.11952C= , LRG_1:g.11952C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1461+33C= MANE Select ENSP00000225964.6:n.1461+33C=
ENST00000225964.9:c.1461+33C= ENSP00000225964.5:n.1461+33C=
ENST00000471344.1:n.405+33C=
NM_000088.3:c.1461+33C= , LRG_1t1:c.1461+33C= NP_000079.2:n.1461+33C=
XM_005257058.3:c.1461+33C= XP_005257115.2:n.1461+33C=
XM_005257059.3:c.957+1626C= XP_005257116.2:n.957+1626C=
XM_011524341.1:c.1263+33C= XP_011522643.1:n.1263+33C=
XM_005257058.4:c.1461+33C= XP_005257115.2:n.1461+33C=
XM_005257059.4:c.957+1626C= XP_005257116.2:n.957+1626C=
NM_000088.4:c.1461+33C= MANE Select NP_000079.2:n.1461+33C=