Canonical Allele Identifier: CA400222084
Community Standard Title: NM_000088.4(COL1A1):c.887G>C (p.Gly296Ala)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50196500C>G , CM000679.2:g.50196500C>G GRCh38
NC_000017.10:g.48273861C>G , CM000679.1:g.48273861C>G GRCh37
NC_000017.9:g.45628860C>G NCBI36
NG_007400.1:g.10140G>C , LRG_1:g.10140G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.887G>C MANE Select NP_000079.2:p.Gly296Ala
ENST00000225964.10:c.887G>C MANE Select ENSP00000225964.6:p.Gly296Ala
NM_000088.3:c.887G>C , LRG_1t1:c.887G>C NP_000079.2:p.Gly296Ala
ENST00000225964.9:c.887G>C ENSP00000225964.5:p.Gly296Ala
ENST00000485870.1:n.96G>C
XM_005257058.3:c.887G>C XP_005257115.2:p.Gly296Ala
XM_005257058.4:c.887G>C XP_005257115.2:p.Gly296Ala
XM_005257059.3:c.887G>C XP_005257116.2:p.Gly296Ala
XM_005257059.4:c.887G>C XP_005257116.2:p.Gly296Ala
XM_011524341.1:c.887G>C XP_011522643.1:p.Gly296Ala