Canonical Allele Identifier: CA2263917791
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50193637A= , CM000679.2:g.50193637A= GRCh38
NC_000017.10:g.48270998A= , CM000679.1:g.48270998A= GRCh37
NC_000017.9:g.45625997A= NCBI36
NG_007400.1:g.13003T= , LRG_1:g.13003T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1767+306T= MANE Select ENSP00000225964.6:n.1767+306T=
ENST00000225964.9:c.1767+306T= ENSP00000225964.5:n.1767+306T=
ENST00000463440.1:n.463T=
ENST00000471344.1:n.1105T=
ENST00000476387.1:n.116+306T=
NM_000088.3:c.1767+306T= , LRG_1t1:c.1767+306T= NP_000079.2:n.1767+306T=
XM_005257058.3:c.1767+306T= XP_005257115.2:n.1767+306T=
XM_005257059.3:c.958-944T= XP_005257116.2:n.958-944T=
XM_011524341.1:c.1569+306T= XP_011522643.1:n.1569+306T=
XM_005257058.4:c.1767+306T= XP_005257115.2:n.1767+306T=
XM_005257059.4:c.958-944T= XP_005257116.2:n.958-944T=
NM_000088.4:c.1767+306T= MANE Select NP_000079.2:n.1767+306T=