Canonical Allele Identifier: CA400222709
Community Standard Title: NM_000088.4(COL1A1):c.806G>A (p.Gly269Asp)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196669C>T , CM000679.2:g.50196669C>T GRCh38
NC_000017.10:g.48274030C>T , CM000679.1:g.48274030C>T GRCh37
NC_000017.9:g.45629029C>T NCBI36
NG_007400.1:g.9971G>A , LRG_1:g.9971G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.806G>A MANE Select NP_000079.2:p.Gly269Asp
ENST00000225964.10:c.806G>A MANE Select ENSP00000225964.6:p.Gly269Asp
NM_000088.3:c.806G>A , LRG_1t1:c.806G>A NP_000079.2:p.Gly269Asp
ENST00000225964.9:c.806G>A ENSP00000225964.5:p.Gly269Asp
ENST00000495677.1:n.533G>A
XM_005257058.3:c.806G>A XP_005257115.2:p.Gly269Asp
XM_005257058.4:c.806G>A XP_005257115.2:p.Gly269Asp
XM_005257059.3:c.806G>A XP_005257116.2:p.Gly269Asp
XM_005257059.4:c.806G>A XP_005257116.2:p.Gly269Asp
XM_011524341.1:c.806G>A XP_011522643.1:p.Gly269Asp