Canonical Allele Identifier: CA2263918080
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194232A= , CM000679.2:g.50194232A= GRCh38
NC_000017.10:g.48271593A= , CM000679.1:g.48271593A= GRCh37
NC_000017.9:g.45626592A= NCBI36
NG_007400.1:g.12408T= , LRG_1:g.12408T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1615-49T= MANE Select ENSP00000225964.6:n.1615-49T=
ENST00000225964.9:c.1615-49T= ENSP00000225964.5:n.1615-49T=
ENST00000463440.1:n.5-49T=
ENST00000471344.1:n.559-49T=
NM_000088.3:c.1615-49T= , LRG_1t1:c.1615-49T= NP_000079.2:n.1615-49T=
XM_005257058.3:c.1615-49T= XP_005257115.2:n.1615-49T=
XM_005257059.3:c.958-1539T= XP_005257116.2:n.958-1539T=
XM_011524341.1:c.1417-49T= XP_011522643.1:n.1417-49T=
XM_005257058.4:c.1615-49T= XP_005257115.2:n.1615-49T=
XM_005257059.4:c.958-1539T= XP_005257116.2:n.958-1539T=
NM_000088.4:c.1615-49T= MANE Select NP_000079.2:n.1615-49T=