Canonical Allele Identifier: CA2263920702
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199415T= , CM000679.2:g.50199415T= GRCh38
NC_000017.10:g.48276776T= , CM000679.1:g.48276776T= GRCh37
NC_000017.9:g.45631775T= NCBI36
NG_007400.1:g.7225A= , LRG_1:g.7225A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.369+3A= MANE Select ENSP00000225964.6:n.369+3A=
ENST00000225964.9:c.369+3A= ENSP00000225964.5:n.369+3A=
ENST00000474644.1:n.590+3A=
ENST00000507689.1:c.423+3A= ENSP00000460459.1:n.423+3A=
NM_000088.3:c.369+3A= , LRG_1t1:c.369+3A= NP_000079.2:n.369+3A=
XM_005257058.3:c.369+3A= XP_005257115.2:n.369+3A=
XM_005257059.3:c.369+3A= XP_005257116.2:n.369+3A=
XM_011524341.1:c.369+3A= XP_011522643.1:n.369+3A=
XM_005257058.4:c.369+3A= XP_005257115.2:n.369+3A=
XM_005257059.4:c.369+3A= XP_005257116.2:n.369+3A=
NM_000088.4:c.369+3A= MANE Select NP_000079.2:n.369+3A=