Canonical Allele Identifier: CA257842
Gene: COL1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17296
dbSNP Id: rs66523073

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50188777C>T , CM000679.2:g.50188777C>T GRCh38
NC_000017.10:g.48266138C>T , CM000679.1:g.48266138C>T GRCh37
NC_000017.9:g.45621137C>T NCBI36
NG_007400.1:g.17863G>A , LRG_1:g.17863G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.3064G>A MANE Select ENSP00000225964.6:p.Gly1022Ser
ENST00000225964.9:c.3064G>A ENSP00000225964.5:p.Gly1022Ser
ENST00000511732.1:n.8G>A
NM_000088.3:c.3064G>A , LRG_1t1:c.3064G>A NP_000079.2:p.Gly1022Ser
XM_005257058.3:c.2794G>A XP_005257115.2:p.Gly932Ser
XM_005257059.3:c.2146G>A XP_005257116.2:p.Gly716Ser
XM_011524341.1:c.2866G>A XP_011522643.1:p.Gly956Ser
XM_005257058.4:c.2794G>A XP_005257115.2:p.Gly932Ser
XM_005257059.4:c.2146G>A XP_005257116.2:p.Gly716Ser
NM_000088.4:c.3064G>A MANE Select NP_000079.2:p.Gly1022Ser