Canonical Allele Identifier: CA2263920594
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50199238_50199256delinsAGGGGGTCCGGGAGGTCCG , CM000679.2:g.50199238_50199256delinsAGGGGGTCCGGGAGGTCCG GRCh38
NC_000017.10:g.48276599_48276617delinsAGGGGGTCCGGGAGGTCCG , CM000679.1:g.48276599_48276617delinsAGGGGGTCCGGGAGGTCCG GRCh37
NC_000017.9:g.45631598_45631616delinsAGGGGGTCCGGGAGGTCCG NCBI36
NG_007400.1:g.7384_7402delinsCGGACCTCCCGGACCCCCT , LRG_1:g.7384_7402delinsCGGACCTCCCGGACCCCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000225964.10:c.441_459delinsCGGACCTCCCGGACCCCCT MANE Select ENSP00000225964.6:p.Pro147=
ENST00000225964.9:c.441_459delinsCGGACCTCCCGGACCCCCT ENSP00000225964.5:p.Pro147=
NM_000088.3:c.441_459delinsCGGACCTCCCGGACCCCCT , LRG_1t1:c.441_459delinsCGGACCTCCCGGACCCCCT NP_000079.2:p.Pro147=
XM_005257058.3:c.441_459delinsCGGACCTCCCGGACCCCCT XP_005257115.2:p.Pro147=
XM_005257059.3:c.441_459delinsCGGACCTCCCGGACCCCCT XP_005257116.2:p.Pro147=
XM_011524341.1:c.441_459delinsCGGACCTCCCGGACCCCCT XP_011522643.1:p.Pro147=
XM_005257058.4:c.441_459delinsCGGACCTCCCGGACCCCCT XP_005257115.2:p.Pro147=
XM_005257059.4:c.441_459delinsCGGACCTCCCGGACCCCCT XP_005257116.2:p.Pro147=
NM_000088.4:c.441_459delinsCGGACCTCCCGGACCCCCT MANE Select NP_000079.2:p.Pro147=