Canonical Allele Identifier: CA2580094130
Gene: COL1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17325
ClinVar RCV Id: RCV000018866
dbSNP Id: rs2144577336

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195599_50196327dup , CM000679.2:g.50195599_50196327dup GRCh38
NC_000017.10:g.48272960_48273688dup , CM000679.1:g.48272960_48273688dup GRCh37
NC_000017.9:g.45627959_45628687dup NCBI36
NG_007400.1:g.10328_11056dup , LRG_1:g.10328_11056dup

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.957+2_1138dup
ENST00000225964.9:c.957+2_1138dup
NM_000088.3:c.957+2_1138dup , LRG_1t1:c.957+2_1138dup
XM_005257058.3:c.957+2_1138dup
XM_005257059.3:c.957+2_957+730dup
XM_011524341.1:c.957+2_958-106dup
XM_005257058.4:c.957+2_1138dup
XM_005257059.4:c.957+2_957+730dup
NM_000088.4:c.957+2_1138dup