Canonical Allele Identifier: CA8644872
Community Standard Title: NM_000088.4(COL1A1):c.2323G>A (p.Ala775Thr)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50190837C>T , CM000679.2:g.50190837C>T GRCh38
NC_000017.10:g.48268198C>T , CM000679.1:g.48268198C>T GRCh37
NC_000017.9:g.45623197C>T NCBI36
NG_007400.1:g.15803G>A , LRG_1:g.15803G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.2323G>A MANE Select NP_000079.2:p.Ala775Thr
ENST00000225964.10:c.2323G>A MANE Select ENSP00000225964.6:p.Ala775Thr
NM_000088.3:c.2323G>A , LRG_1t1:c.2323G>A NP_000079.2:p.Ala775Thr
ENST00000225964.9:c.2323G>A ENSP00000225964.5:p.Ala775Thr
ENST00000494334.1:n.88G>A
XM_005257058.3:c.2323G>A XP_005257115.2:p.Ala775Thr
XM_005257058.4:c.2323G>A XP_005257115.2:p.Ala775Thr
XM_005257059.3:c.1405G>A XP_005257116.2:p.Ala469Thr
XM_005257059.4:c.1405G>A XP_005257116.2:p.Ala469Thr
XM_011524341.1:c.2125G>A XP_011522643.1:p.Ala709Thr