Canonical Allele Identifier: CA2263917895
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50193846G= , CM000679.2:g.50193846G= GRCh38
NC_000017.10:g.48271207G= , CM000679.1:g.48271207G= GRCh37
NC_000017.9:g.45626206G= NCBI36
NG_007400.1:g.12794C= , LRG_1:g.12794C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1767+97C= MANE Select ENSP00000225964.6:n.1767+97C=
ENST00000225964.9:c.1767+97C= ENSP00000225964.5:n.1767+97C=
ENST00000463440.1:n.254C=
ENST00000471344.1:n.896C=
ENST00000476387.1:n.116+97C=
NM_000088.3:c.1767+97C= , LRG_1t1:c.1767+97C= NP_000079.2:n.1767+97C=
XM_005257058.3:c.1767+97C= XP_005257115.2:n.1767+97C=
XM_005257059.3:c.958-1153C= XP_005257116.2:n.958-1153C=
XM_011524341.1:c.1569+97C= XP_011522643.1:n.1569+97C=
XM_005257058.4:c.1767+97C= XP_005257115.2:n.1767+97C=
XM_005257059.4:c.958-1153C= XP_005257116.2:n.958-1153C=
NM_000088.4:c.1767+97C= MANE Select NP_000079.2:n.1767+97C=