Canonical Allele Identifier: CA1139665708
Gene: COL1A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 955441
ClinVar RCV Id: RCV001228084
dbSNP Id: rs1907543361

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195936_50195937dup , CM000679.2:g.50195936_50195937dup GRCh38
NC_000017.10:g.48273297_48273298dup , CM000679.1:g.48273297_48273298dup GRCh37
NC_000017.9:g.45628296_45628297dup NCBI36
NG_007400.1:g.10703_10704dup , LRG_1:g.10703_10704dup

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.1042_1043dup MANE Select ENSP00000225964.6:p.Val349LeufsTer?
ENST00000225964.9:c.1042_1043dup ENSP00000225964.5:p.Val349LeufsTer?
NM_000088.3:c.1042_1043dup , LRG_1t1:c.1042_1043dup NP_000079.2:p.Val349LeufsTer?
XM_005257058.3:c.1042_1043dup XP_005257115.2:p.Val349LeufsTer?
XM_005257059.3:c.957+377_957+378dup XP_005257116.2:n.957+377_957+378dup
XM_011524341.1:c.957+377_957+378dup XP_011522643.1:n.957+377_957+378dup
XM_005257058.4:c.1042_1043dup XP_005257115.2:p.Val349LeufsTer?
XM_005257059.4:c.957+377_957+378dup XP_005257116.2:n.957+377_957+378dup
NM_000088.4:c.1042_1043dup MANE Select NP_000079.2:p.Val349LeufsTer?