Canonical Allele Identifier: CA500848481
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48271355A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50193994A>G , CM000679.2:g.50193994A>G GRCh38
NC_000017.10:g.48271355A>G , CM000679.1:g.48271355A>G GRCh37
NC_000017.9:g.45626354A>G NCBI36
NG_007400.1:g.12646T>C , LRG_1:g.12646T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.1716T>C MANE Select ENSP00000225964.6:p.Gly572=
ENST00000225964.9:c.1716T>C ENSP00000225964.5:p.Gly572=
ENST00000463440.1:n.106T>C
ENST00000471344.1:n.748T>C
ENST00000476387.1:n.65T>C
NM_000088.3:c.1716T>C , LRG_1t1:c.1716T>C NP_000079.2:p.Gly572=
XM_005257058.3:c.1716T>C XP_005257115.2:p.Gly572=
XM_005257059.3:c.958-1301T>C XP_005257116.2:n.958-1301T>C
XM_011524341.1:c.1518T>C XP_011522643.1:p.Gly506=
XM_005257058.4:c.1716T>C XP_005257115.2:p.Gly572=
XM_005257059.4:c.958-1301T>C XP_005257116.2:n.958-1301T>C
NM_000088.4:c.1716T>C MANE Select NP_000079.2:p.Gly572=