Canonical Allele Identifier: CA400218721
Community Standard Title: NM_000088.4(COL1A1):c.1261C>T (p.Gln421Ter)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195270G>A , CM000679.2:g.50195270G>A GRCh38
NC_000017.10:g.48272631G>A , CM000679.1:g.48272631G>A GRCh37
NC_000017.9:g.45627630G>A NCBI36
NG_007400.1:g.11370C>T , LRG_1:g.11370C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.1261C>T MANE Select NP_000079.2:p.Gln421Ter
ENST00000225964.10:c.1261C>T MANE Select ENSP00000225964.6:p.Gln421Ter
NM_000088.3:c.1261C>T , LRG_1t1:c.1261C>T NP_000079.2:p.Gln421Ter
ENST00000225964.9:c.1261C>T ENSP00000225964.5:p.Gln421Ter
ENST00000471344.1:n.205C>T
XM_005257058.3:c.1261C>T XP_005257115.2:p.Gln421Ter
XM_005257058.4:c.1261C>T XP_005257115.2:p.Gln421Ter
XM_005257059.3:c.957+1044C>T XP_005257116.2:n.957+1044C>T
XM_005257059.4:c.957+1044C>T XP_005257116.2:n.957+1044C>T
XM_011524341.1:c.1063C>T XP_011522643.1:p.Gln355Ter