Canonical Allele Identifier: CA2263917812
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50193689G= , CM000679.2:g.50193689G= GRCh38
NC_000017.10:g.48271050G= , CM000679.1:g.48271050G= GRCh37
NC_000017.9:g.45626049G= NCBI36
NG_007400.1:g.12951C= , LRG_1:g.12951C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1767+254C= MANE Select ENSP00000225964.6:n.1767+254C=
ENST00000225964.9:c.1767+254C= ENSP00000225964.5:n.1767+254C=
ENST00000463440.1:n.411C=
ENST00000471344.1:n.1053C=
ENST00000476387.1:n.116+254C=
NM_000088.3:c.1767+254C= , LRG_1t1:c.1767+254C= NP_000079.2:n.1767+254C=
XM_005257058.3:c.1767+254C= XP_005257115.2:n.1767+254C=
XM_005257059.3:c.958-996C= XP_005257116.2:n.958-996C=
XM_011524341.1:c.1569+254C= XP_011522643.1:n.1569+254C=
XM_005257058.4:c.1767+254C= XP_005257115.2:n.1767+254C=
XM_005257059.4:c.958-996C= XP_005257116.2:n.958-996C=
NM_000088.4:c.1767+254C= MANE Select NP_000079.2:n.1767+254C=