Canonical Allele Identifier: CA400227637
Community Standard Title: NM_000088.4(COL1A1):c.358C>T (p.Arg120Ter)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199429G>A , CM000679.2:g.50199429G>A GRCh38
NC_000017.10:g.48276790G>A , CM000679.1:g.48276790G>A GRCh37
NC_000017.9:g.45631789G>A NCBI36
NG_007400.1:g.7211C>T , LRG_1:g.7211C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.358C>T MANE Select NP_000079.2:p.Arg120Ter
ENST00000225964.10:c.358C>T MANE Select ENSP00000225964.6:p.Arg120Ter
NM_000088.3:c.358C>T , LRG_1t1:c.358C>T NP_000079.2:p.Arg120Ter
ENST00000225964.9:c.358C>T ENSP00000225964.5:p.Arg120Ter
ENST00000474644.1:n.579C>T
ENST00000507689.1:c.412C>T ENSP00000460459.1:p.Arg138Ter
XM_005257058.3:c.358C>T XP_005257115.2:p.Arg120Ter
XM_005257058.4:c.358C>T XP_005257115.2:p.Arg120Ter
XM_005257059.3:c.358C>T XP_005257116.2:p.Arg120Ter
XM_005257059.4:c.358C>T XP_005257116.2:p.Arg120Ter
XM_011524341.1:c.358C>T XP_011522643.1:p.Arg120Ter