Canonical Allele Identifier: CA10588662
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50187067C>T , CM000679.2:g.50187067C>T GRCh38
NC_000017.10:g.48264428C>T , CM000679.1:g.48264428C>T GRCh37
NC_000017.9:g.45619427C>T NCBI36
NG_007400.1:g.19573G>A , LRG_1:g.19573G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.3479G>A MANE Select ENSP00000225964.6:p.Gly1160Asp
ENST00000225964.9:c.3479G>A ENSP00000225964.5:p.Gly1160Asp
ENST00000510710.3:n.56G>A
NM_000088.3:c.3479G>A , LRG_1t1:c.3479G>A NP_000079.2:p.Gly1160Asp
XM_005257058.3:c.3209G>A XP_005257115.2:p.Gly1070Asp
XM_005257059.3:c.2561G>A XP_005257116.2:p.Gly854Asp
XM_011524341.1:c.3281G>A XP_011522643.1:p.Gly1094Asp
XM_005257058.4:c.3209G>A XP_005257115.2:p.Gly1070Asp
XM_005257059.4:c.2561G>A XP_005257116.2:p.Gly854Asp
NM_000088.4:c.3479G>A MANE Select NP_000079.2:p.Gly1160Asp