Canonical Allele Identifier: CA2263920689
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199394C= , CM000679.2:g.50199394C= GRCh38
NC_000017.10:g.48276755C= , CM000679.1:g.48276755C= GRCh37
NC_000017.9:g.45631754C= NCBI36
NG_007400.1:g.7246G= , LRG_1:g.7246G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.369+24G= MANE Select ENSP00000225964.6:n.369+24G=
ENST00000225964.9:c.369+24G= ENSP00000225964.5:n.369+24G=
ENST00000474644.1:n.590+24G=
ENST00000507689.1:c.423+24G= ENSP00000460459.1:n.423+24G=
NM_000088.3:c.369+24G= , LRG_1t1:c.369+24G= NP_000079.2:n.369+24G=
XM_005257058.3:c.369+24G= XP_005257115.2:n.369+24G=
XM_005257059.3:c.369+24G= XP_005257116.2:n.369+24G=
XM_011524341.1:c.369+24G= XP_011522643.1:n.369+24G=
XM_005257058.4:c.369+24G= XP_005257115.2:n.369+24G=
XM_005257059.4:c.369+24G= XP_005257116.2:n.369+24G=
NM_000088.4:c.369+24G= MANE Select NP_000079.2:n.369+24G=