Canonical Allele Identifier: CA8644938
Community Standard Title: NM_000088.4(COL1A1):c.2090G>A (p.Arg697Gln)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50191825C>T , CM000679.2:g.50191825C>T GRCh38
NC_000017.10:g.48269186C>T , CM000679.1:g.48269186C>T GRCh37
NC_000017.9:g.45624185C>T NCBI36
NG_007400.1:g.14815G>A , LRG_1:g.14815G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.2090G>A MANE Select NP_000079.2:p.Arg697Gln
ENST00000225964.10:c.2090G>A MANE Select ENSP00000225964.6:p.Arg697Gln
NM_000088.3:c.2090G>A , LRG_1t1:c.2090G>A NP_000079.2:p.Arg697Gln
ENST00000225964.9:c.2090G>A ENSP00000225964.5:p.Arg697Gln
ENST00000476387.1:n.439G>A
XM_005257058.3:c.2090G>A XP_005257115.2:p.Arg697Gln
XM_005257058.4:c.2090G>A XP_005257115.2:p.Arg697Gln
XM_005257059.3:c.1172G>A XP_005257116.2:p.Arg391Gln
XM_005257059.4:c.1172G>A XP_005257116.2:p.Arg391Gln
XM_011524341.1:c.1892G>A XP_011522643.1:p.Arg631Gln