Canonical Allele Identifier: CA2263919109
Community Standard Title: NM_000088.4(COL1A1):c.994G= (p.Gly332=)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196163C= , CM000679.2:g.50196163C= GRCh38
NC_000017.10:g.48273524C= , CM000679.1:g.48273524C= GRCh37
NC_000017.9:g.45628523C= NCBI36
NG_007400.1:g.10477G= , LRG_1:g.10477G=

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.994G= MANE Select NP_000079.2:p.Gly332=
ENST00000225964.10:c.994G= MANE Select ENSP00000225964.6:p.Gly332=
NM_000088.3:c.994G= , LRG_1t1:c.994G= NP_000079.2:p.Gly332=
ENST00000225964.9:c.994G= ENSP00000225964.5:p.Gly332=
ENST00000485870.1:n.319G=
XM_005257058.3:c.994G= XP_005257115.2:p.Gly332=
XM_005257058.4:c.994G= XP_005257115.2:p.Gly332=
XM_005257059.3:c.957+151G= XP_005257116.2:n.957+151G=
XM_005257059.4:c.957+151G= XP_005257116.2:n.957+151G=
XM_011524341.1:c.957+151G= XP_011522643.1:n.957+151G=