Canonical Allele Identifier: CA8644357
Community Standard Title: NM_000088.4(COL1A1):c.3769C>T (p.Arg1257Cys)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50186685G>A , CM000679.2:g.50186685G>A GRCh38
NC_000017.10:g.48264046G>A , CM000679.1:g.48264046G>A GRCh37
NC_000017.9:g.45619045G>A NCBI36
NG_007400.1:g.19955C>T , LRG_1:g.19955C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.3769C>T MANE Select NP_000079.2:p.Arg1257Cys
ENST00000225964.10:c.3769C>T MANE Select ENSP00000225964.6:p.Arg1257Cys
NM_000088.3:c.3769C>T , LRG_1t1:c.3769C>T NP_000079.2:p.Arg1257Cys
ENST00000225964.9:c.3769C>T ENSP00000225964.5:p.Arg1257Cys
ENST00000510710.3:n.438C>T
XM_005257058.3:c.3499C>T XP_005257115.2:p.Arg1167Cys
XM_005257058.4:c.3499C>T XP_005257115.2:p.Arg1167Cys
XM_005257059.3:c.2851C>T XP_005257116.2:p.Arg951Cys
XM_005257059.4:c.2851C>T XP_005257116.2:p.Arg951Cys
XM_011524341.1:c.3571C>T XP_011522643.1:p.Arg1191Cys