Canonical Allele Identifier: CA500848817
Gene: COL1A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48271536A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50194175A>G , CM000679.2:g.50194175A>G GRCh38
NC_000017.10:g.48271536A>G , CM000679.1:g.48271536A>G GRCh37
NC_000017.9:g.45626535A>G NCBI36
NG_007400.1:g.12465T>C , LRG_1:g.12465T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1623T>C MANE Select ENSP00000225964.6:p.Thr541=
ENST00000225964.9:c.1623T>C ENSP00000225964.5:p.Thr541=
ENST00000463440.1:n.13T>C
ENST00000471344.1:n.567T>C
NM_000088.3:c.1623T>C , LRG_1t1:c.1623T>C NP_000079.2:p.Thr541=
XM_005257058.3:c.1623T>C XP_005257115.2:p.Thr541=
XM_005257059.3:c.958-1482T>C XP_005257116.2:n.958-1482T>C
XM_011524341.1:c.1425T>C XP_011522643.1:p.Thr475=
XM_005257058.4:c.1623T>C XP_005257115.2:p.Thr541=
XM_005257059.4:c.958-1482T>C XP_005257116.2:n.958-1482T>C
NM_000088.4:c.1623T>C MANE Select NP_000079.2:p.Thr541=