Canonical Allele Identifier: CA400198911
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs72656321

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50187094C>T , CM000679.2:g.50187094C>T GRCh38
NC_000017.10:g.48264455C>T , CM000679.1:g.48264455C>T GRCh37
NC_000017.9:g.45619454C>T NCBI36
NG_007400.1:g.19546G>A , LRG_1:g.19546G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.3452G>A MANE Select ENSP00000225964.6:p.Gly1151Asp
ENST00000225964.9:c.3452G>A ENSP00000225964.5:p.Gly1151Asp
ENST00000510710.3:n.29G>A
NM_000088.3:c.3452G>A , LRG_1t1:c.3452G>A NP_000079.2:p.Gly1151Asp
XM_005257058.3:c.3182G>A XP_005257115.2:p.Gly1061Asp
XM_005257059.3:c.2534G>A XP_005257116.2:p.Gly845Asp
XM_011524341.1:c.3254G>A XP_011522643.1:p.Gly1085Asp
XM_005257058.4:c.3182G>A XP_005257115.2:p.Gly1061Asp
XM_005257059.4:c.2534G>A XP_005257116.2:p.Gly845Asp
NM_000088.4:c.3452G>A MANE Select NP_000079.2:p.Gly1151Asp