Canonical Allele Identifier: CA500842814
Gene: COL1A1 HGNC NCBI

Linked Data

dbSNP Id: rs891380309
MyVariant Identifiers: chr17:g.48262911G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50185550G>T , CM000679.2:g.50185550G>T GRCh38
NC_000017.10:g.48262911G>T , CM000679.1:g.48262911G>T GRCh37
NC_000017.9:g.45617910G>T NCBI36
NG_007400.1:g.21090C>A , LRG_1:g.21090C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.4347C>A MANE Select ENSP00000225964.6:p.Ala1449=
ENST00000225964.9:c.4347C>A ENSP00000225964.5:p.Ala1449=
NM_000088.3:c.4347C>A , LRG_1t1:c.4347C>A NP_000079.2:p.Ala1449=
XM_005257058.3:c.4077C>A XP_005257115.2:p.Ala1359=
XM_005257059.3:c.3429C>A XP_005257116.2:p.Ala1143=
XM_011524341.1:c.4149C>A XP_011522643.1:p.Ala1383=
XM_005257058.4:c.4077C>A XP_005257115.2:p.Ala1359=
XM_005257059.4:c.3429C>A XP_005257116.2:p.Ala1143=
NM_000088.4:c.4347C>A MANE Select NP_000079.2:p.Ala1449=