Canonical Allele Identifier: CA2263918156
Community Standard Title: NM_000088.4(COL1A1):c.1583G= (p.Arg528=)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194380C= , CM000679.2:g.50194380C= GRCh38
NC_000017.10:g.48271741C= , CM000679.1:g.48271741C= GRCh37
NC_000017.9:g.45626740C= NCBI36
NG_007400.1:g.12260G= , LRG_1:g.12260G=

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.1583G= MANE Select NP_000079.2:p.Arg528=
ENST00000225964.10:c.1583G= MANE Select ENSP00000225964.6:p.Arg528=
NM_000088.3:c.1583G= , LRG_1t1:c.1583G= NP_000079.2:p.Arg528=
ENST00000225964.9:c.1583G= ENSP00000225964.5:p.Arg528=
ENST00000471344.1:n.527G=
XM_005257058.3:c.1583G= XP_005257115.2:p.Arg528=
XM_005257058.4:c.1583G= XP_005257115.2:p.Arg528=
XM_005257059.3:c.958-1687G= XP_005257116.2:n.958-1687G=
XM_005257059.4:c.958-1687G= XP_005257116.2:n.958-1687G=
XM_011524341.1:c.1385G= XP_011522643.1:p.Arg462=