Canonical Allele Identifier: CA400199802
Community Standard Title: NM_000088.4(COL1A1):c.3304C>T (p.Gln1102Ter)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50187941G>A , CM000679.2:g.50187941G>A GRCh38
NC_000017.10:g.48265302G>A , CM000679.1:g.48265302G>A GRCh37
NC_000017.9:g.45620301G>A NCBI36
NG_007400.1:g.18699C>T , LRG_1:g.18699C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.3304C>T MANE Select NP_000079.2:p.Gln1102Ter
ENST00000225964.10:c.3304C>T MANE Select ENSP00000225964.6:p.Gln1102Ter
NM_000088.3:c.3304C>T , LRG_1t1:c.3304C>T NP_000079.2:p.Gln1102Ter
ENST00000225964.9:c.3304C>T ENSP00000225964.5:p.Gln1102Ter
ENST00000486572.1:n.502C>T
ENST00000511732.1:n.740C>T
XM_005257058.3:c.3034C>T XP_005257115.2:p.Gln1012Ter
XM_005257058.4:c.3034C>T XP_005257115.2:p.Gln1012Ter
XM_005257059.3:c.2386C>T XP_005257116.2:p.Gln796Ter
XM_005257059.4:c.2386C>T XP_005257116.2:p.Gln796Ter
XM_011524341.1:c.3106C>T XP_011522643.1:p.Gln1036Ter