Canonical Allele Identifier: CA291547038
Community Standard Title: NM_000088.4(COL1A1):c.1011C>T (p.Thr337=)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195968G>A , CM000679.2:g.50195968G>A GRCh38
NC_000017.10:g.48273329G>A , CM000679.1:g.48273329G>A GRCh37
NC_000017.9:g.45628328G>A NCBI36
NG_007400.1:g.10672C>T , LRG_1:g.10672C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.1011C>T MANE Select NP_000079.2:p.Thr337=
ENST00000225964.10:c.1011C>T MANE Select ENSP00000225964.6:p.Thr337=
NM_000088.3:c.1011C>T , LRG_1t1:c.1011C>T NP_000079.2:p.Thr337=
ENST00000225964.9:c.1011C>T ENSP00000225964.5:p.Thr337=
XM_005257058.3:c.1011C>T XP_005257115.2:p.Thr337=
XM_005257058.4:c.1011C>T XP_005257115.2:p.Thr337=
XM_005257059.3:c.957+346C>T XP_005257116.2:n.957+346C>T
XM_005257059.4:c.957+346C>T XP_005257116.2:n.957+346C>T
XM_011524341.1:c.957+346C>T XP_011522643.1:n.957+346C>T