Canonical Allele Identifier: CA500848845
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48271542A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194181A>T , CM000679.2:g.50194181A>T GRCh38
NC_000017.10:g.48271542A>T , CM000679.1:g.48271542A>T GRCh37
NC_000017.9:g.45626541A>T NCBI36
NG_007400.1:g.12459T>A , LRG_1:g.12459T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1617T>A MANE Select ENSP00000225964.6:p.Gly539=
ENST00000225964.9:c.1617T>A ENSP00000225964.5:p.Gly539=
ENST00000463440.1:n.7T>A
ENST00000471344.1:n.561T>A
NM_000088.3:c.1617T>A , LRG_1t1:c.1617T>A NP_000079.2:p.Gly539=
XM_005257058.3:c.1617T>A XP_005257115.2:p.Gly539=
XM_005257059.3:c.958-1488T>A XP_005257116.2:n.958-1488T>A
XM_011524341.1:c.1419T>A XP_011522643.1:p.Gly473=
XM_005257058.4:c.1617T>A XP_005257115.2:p.Gly539=
XM_005257059.4:c.958-1488T>A XP_005257116.2:n.958-1488T>A
NM_000088.4:c.1617T>A MANE Select NP_000079.2:p.Gly539=