Canonical Allele Identifier: CA400198223
Community Standard Title: NM_000088.4(COL1A1):c.3569G>A (p.Gly1190Asp)
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50186885C>T , CM000679.2:g.50186885C>T GRCh38
NC_000017.10:g.48264246C>T , CM000679.1:g.48264246C>T GRCh37
NC_000017.9:g.45619245C>T NCBI36
NG_007400.1:g.19755G>A , LRG_1:g.19755G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000088.4:c.3569G>A MANE Select NP_000079.2:p.Gly1190Asp
ENST00000225964.10:c.3569G>A MANE Select ENSP00000225964.6:p.Gly1190Asp
NM_000088.3:c.3569G>A , LRG_1t1:c.3569G>A NP_000079.2:p.Gly1190Asp
ENST00000225964.9:c.3569G>A ENSP00000225964.5:p.Gly1190Asp
ENST00000510710.3:n.238G>A
XM_005257058.3:c.3299G>A XP_005257115.2:p.Gly1100Asp
XM_005257058.4:c.3299G>A XP_005257115.2:p.Gly1100Asp
XM_005257059.3:c.2651G>A XP_005257116.2:p.Gly884Asp
XM_005257059.4:c.2651G>A XP_005257116.2:p.Gly884Asp
XM_011524341.1:c.3371G>A XP_011522643.1:p.Gly1124Asp