Canonical Allele Identifier: CA400206107
Community Standard Title: NM_000088.4(COL1A1):c.2669G>C (p.Gly890Ala)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50189537C>G , CM000679.2:g.50189537C>G GRCh38
NC_000017.10:g.48266898C>G , CM000679.1:g.48266898C>G GRCh37
NC_000017.9:g.45621897C>G NCBI36
NG_007400.1:g.17103G>C , LRG_1:g.17103G>C

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.2669G>C MANE Select NP_000079.2:p.Gly890Ala
ENST00000225964.10:c.2669G>C MANE Select ENSP00000225964.6:p.Gly890Ala
NM_000088.3:c.2669G>C , LRG_1t1:c.2669G>C NP_000079.2:p.Gly890Ala
ENST00000225964.9:c.2669G>C ENSP00000225964.5:p.Gly890Ala
XM_005257058.3:c.2667+142G>C XP_005257115.2:n.2667+142G>C
XM_005257058.4:c.2667+142G>C XP_005257115.2:n.2667+142G>C
XM_005257059.3:c.1751G>C XP_005257116.2:p.Gly584Ala
XM_005257059.4:c.1751G>C XP_005257116.2:p.Gly584Ala
XM_011524341.1:c.2471G>C XP_011522643.1:p.Gly824Ala