Canonical Allele Identifier: CA2263918839
Gene: COL1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50195633A= , CM000679.2:g.50195633A= GRCh38
NC_000017.10:g.48272994A= , CM000679.1:g.48272994A= GRCh37
NC_000017.9:g.45627993A= NCBI36
NG_007400.1:g.11007T= , LRG_1:g.11007T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225964.10:c.1089T= MANE Select ENSP00000225964.6:p.Ser363=
ENST00000225964.9:c.1089T= ENSP00000225964.5:p.Ser363=
ENST00000471344.1:n.33T=
NM_000088.3:c.1089T= , LRG_1t1:c.1089T= NP_000079.2:p.Ser363=
XM_005257058.3:c.1089T= XP_005257115.2:p.Ser363=
XM_005257059.3:c.957+681T= XP_005257116.2:n.957+681T=
XM_011524341.1:c.958-155T= XP_011522643.1:n.958-155T=
XM_005257058.4:c.1089T= XP_005257115.2:p.Ser363=
XM_005257059.4:c.957+681T= XP_005257116.2:n.957+681T=
NM_000088.4:c.1089T= MANE Select NP_000079.2:p.Ser363=