Canonical Allele Identifier: CA400207705
Community Standard Title: NM_000088.4(COL1A1):c.2507G>A (p.Gly836Asp)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50190053C>T , CM000679.2:g.50190053C>T GRCh38
NC_000017.10:g.48267414C>T , CM000679.1:g.48267414C>T GRCh37
NC_000017.9:g.45622413C>T NCBI36
NG_007400.1:g.16587G>A , LRG_1:g.16587G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.2507G>A MANE Select NP_000079.2:p.Gly836Asp
ENST00000225964.10:c.2507G>A MANE Select ENSP00000225964.6:p.Gly836Asp
NM_000088.3:c.2507G>A , LRG_1t1:c.2507G>A NP_000079.2:p.Gly836Asp
ENST00000225964.9:c.2507G>A ENSP00000225964.5:p.Gly836Asp
XM_005257058.3:c.2507G>A XP_005257115.2:p.Gly836Asp
XM_005257058.4:c.2507G>A XP_005257115.2:p.Gly836Asp
XM_005257059.3:c.1589G>A XP_005257116.2:p.Gly530Asp
XM_005257059.4:c.1589G>A XP_005257116.2:p.Gly530Asp
XM_011524341.1:c.2309G>A XP_011522643.1:p.Gly770Asp