Canonical Allele Identifier: CA2263918321
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194683T= , CM000679.2:g.50194683T= GRCh38
NC_000017.10:g.48272044T= , CM000679.1:g.48272044T= GRCh37
NC_000017.9:g.45627043T= NCBI36
NG_007400.1:g.11957A= , LRG_1:g.11957A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1461+38A= MANE Select ENSP00000225964.6:n.1461+38A=
ENST00000225964.9:c.1461+38A= ENSP00000225964.5:n.1461+38A=
ENST00000471344.1:n.405+38A=
NM_000088.3:c.1461+38A= , LRG_1t1:c.1461+38A= NP_000079.2:n.1461+38A=
XM_005257058.3:c.1461+38A= XP_005257115.2:n.1461+38A=
XM_005257059.3:c.957+1631A= XP_005257116.2:n.957+1631A=
XM_011524341.1:c.1263+38A= XP_011522643.1:n.1263+38A=
XM_005257058.4:c.1461+38A= XP_005257115.2:n.1461+38A=
XM_005257059.4:c.957+1631A= XP_005257116.2:n.957+1631A=
NM_000088.4:c.1461+38A= MANE Select NP_000079.2:n.1461+38A=