Canonical Allele Identifier: CA2263920635
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199309C= , CM000679.2:g.50199309C= GRCh38
NC_000017.10:g.48276670C= , CM000679.1:g.48276670C= GRCh37
NC_000017.9:g.45631669C= NCBI36
NG_007400.1:g.7331G= , LRG_1:g.7331G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.388G= MANE Select ENSP00000225964.6:p.Gly130=
ENST00000225964.9:c.388G= ENSP00000225964.5:p.Gly130=
ENST00000474644.1:n.609G=
ENST00000507689.1:c.442G= ENSP00000460459.1:p.Gly148=
NM_000088.3:c.388G= , LRG_1t1:c.388G= NP_000079.2:p.Gly130=
XM_005257058.3:c.388G= XP_005257115.2:p.Gly130=
XM_005257059.3:c.388G= XP_005257116.2:p.Gly130=
XM_011524341.1:c.388G= XP_011522643.1:p.Gly130=
XM_005257058.4:c.388G= XP_005257115.2:p.Gly130=
XM_005257059.4:c.388G= XP_005257116.2:p.Gly130=
NM_000088.4:c.388G= MANE Select NP_000079.2:p.Gly130=