Canonical Allele Identifier: CA500848030
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48270164G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50192803G>T , CM000679.2:g.50192803G>T GRCh38
NC_000017.10:g.48270164G>T , CM000679.1:g.48270164G>T GRCh37
NC_000017.9:g.45625163G>T NCBI36
NG_007400.1:g.13837C>A , LRG_1:g.13837C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1869C>A MANE Select ENSP00000225964.6:p.Gly623=
ENST00000225964.9:c.1869C>A ENSP00000225964.5:p.Gly623=
ENST00000476387.1:n.218C>A
NM_000088.3:c.1869C>A , LRG_1t1:c.1869C>A NP_000079.2:p.Gly623=
XM_005257058.3:c.1869C>A XP_005257115.2:p.Gly623=
XM_005257059.3:c.958-110C>A XP_005257116.2:n.958-110C>A
XM_011524341.1:c.1671C>A XP_011522643.1:p.Gly557=
XM_005257058.4:c.1869C>A XP_005257115.2:p.Gly623=
XM_005257059.4:c.958-110C>A XP_005257116.2:n.958-110C>A
NM_000088.4:c.1869C>A MANE Select NP_000079.2:p.Gly623=