Canonical Allele Identifier: CA2263916127
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50190293G= , CM000679.2:g.50190293G= GRCh38
NC_000017.10:g.48267654G= , CM000679.1:g.48267654G= GRCh37
NC_000017.9:g.45622653G= NCBI36
NG_007400.1:g.16347C= , LRG_1:g.16347C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.2451+34C= MANE Select ENSP00000225964.6:n.2451+34C=
ENST00000225964.9:c.2451+34C= ENSP00000225964.5:n.2451+34C=
NM_000088.3:c.2451+34C= , LRG_1t1:c.2451+34C= NP_000079.2:n.2451+34C=
XM_005257058.3:c.2451+34C= XP_005257115.2:n.2451+34C=
XM_005257059.3:c.1533+34C= XP_005257116.2:n.1533+34C=
XM_011524341.1:c.2253+34C= XP_011522643.1:n.2253+34C=
XM_005257058.4:c.2451+34C= XP_005257115.2:n.2451+34C=
XM_005257059.4:c.1533+34C= XP_005257116.2:n.1533+34C=
NM_000088.4:c.2451+34C= MANE Select NP_000079.2:n.2451+34C=