Canonical Allele Identifier: CA8644911
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50191443G>A , CM000679.2:g.50191443G>A GRCh38
NC_000017.10:g.48268804G>A , CM000679.1:g.48268804G>A GRCh37
NC_000017.9:g.45623803G>A NCBI36
NG_007400.1:g.15197C>T , LRG_1:g.15197C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.2175C>T MANE Select ENSP00000225964.6:p.Gly725=
ENST00000225964.9:c.2175C>T ENSP00000225964.5:p.Gly725=
ENST00000476387.1:n.524C>T
NM_000088.3:c.2175C>T , LRG_1t1:c.2175C>T NP_000079.2:p.Gly725=
XM_005257058.3:c.2175C>T XP_005257115.2:p.Gly725=
XM_005257059.3:c.1257C>T XP_005257116.2:p.Gly419=
XM_011524341.1:c.1977C>T XP_011522643.1:p.Gly659=
XM_005257058.4:c.2175C>T XP_005257115.2:p.Gly725=
XM_005257059.4:c.1257C>T XP_005257116.2:p.Gly419=
NM_000088.4:c.2175C>T MANE Select NP_000079.2:p.Gly725=