Canonical Allele Identifier: CA2573154197

Gene: COL1A1

Linked Data

• ClinVar Variation Id: 1373359
• ClinVar RCV Id: RCV001880730
• dbSNP Id: rs2144545163

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.50188526T>A , CM000679.2:g.50188526T>A	GRCh38
NC_000017.10:g.48265887T>A , CM000679.1:g.48265887T>A	GRCh37
NC_000017.9:g.45620886T>A	NCBI36
NG_007400.1:g.18114A>T , LRG_1:g.18114A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225964.10:c.3207+4A>T MANE Select	ENSP00000225964.6:n.3207+4A>T
ENST00000225964.9:c.3207+4A>T	ENSP00000225964.5:n.3207+4A>T
ENST00000486572.1:n.29A>T
ENST00000511732.1:n.155A>T
NM_000088.3:c.3207+4A>T , LRG_1t1:c.3207+4A>T	NP_000079.2:n.3207+4A>T
XM_005257058.3:c.2937+4A>T	XP_005257115.2:n.2937+4A>T
XM_005257059.3:c.2289+4A>T	XP_005257116.2:n.2289+4A>T
XM_011524341.1:c.3009+4A>T	XP_011522643.1:n.3009+4A>T
XM_005257058.4:c.2937+4A>T	XP_005257115.2:n.2937+4A>T
XM_005257059.4:c.2289+4A>T	XP_005257116.2:n.2289+4A>T
NM_000088.4:c.3207+4A>T MANE Select	NP_000079.2:n.3207+4A>T