Canonical Allele Identifier: CA500852219
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48276686T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199325T>G , CM000679.2:g.50199325T>G GRCh38
NC_000017.10:g.48276686T>G , CM000679.1:g.48276686T>G GRCh37
NC_000017.9:g.45631685T>G NCBI36
NG_007400.1:g.7315A>C , LRG_1:g.7315A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.372A>C MANE Select ENSP00000225964.6:p.Gly124=
ENST00000225964.9:c.372A>C ENSP00000225964.5:p.Gly124=
ENST00000474644.1:n.593A>C
ENST00000507689.1:c.426A>C ENSP00000460459.1:p.Gly142=
NM_000088.3:c.372A>C , LRG_1t1:c.372A>C NP_000079.2:p.Gly124=
XM_005257058.3:c.372A>C XP_005257115.2:p.Gly124=
XM_005257059.3:c.372A>C XP_005257116.2:p.Gly124=
XM_011524341.1:c.372A>C XP_011522643.1:p.Gly124=
XM_005257058.4:c.372A>C XP_005257115.2:p.Gly124=
XM_005257059.4:c.372A>C XP_005257116.2:p.Gly124=
NM_000088.4:c.372A>C MANE Select NP_000079.2:p.Gly124=