Canonical Allele Identifier: CA1809060822
Community Standard Title: NM_001146.5(ANGPT1):c.298-18576T=
Gene: ANGPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.107365673A= , CM000670.2:g.107365673A= GRCh38
NC_000008.10:g.108377901A= , CM000670.1:g.108377901A= GRCh37
NC_000008.9:g.108447077A= NCBI36
NG_029405.1:g.137354T=

Transcript Alleles

HGVS Amino-acid Change
NM_001146.5:c.298-18576T= MANE Select NP_001137.2:n.298-18576T=
ENST00000517746.6:c.298-18576T= MANE Select ENSP00000428340.1:n.298-18576T=
NM_001146.3:c.298-18576T= NP_001137.2:n.298-18576T=
NM_001146.4:c.298-18576T= NP_001137.2:n.298-18576T=
NM_001199859.1:c.298-18576T= NP_001186788.1:n.298-18576T=
NM_001199859.2:c.298-18576T= NP_001186788.1:n.298-18576T=
NM_001199859.3:c.298-18576T= NP_001186788.1:n.298-18576T=
ENST00000297450.7:c.298-18576T= ENSP00000297450.3:n.298-18576T=
ENST00000517746.5:c.298-18576T= ENSP00000428340.1:n.298-18576T=
ENST00000520033.1:c.-24-18576T= ENSP00000428908.1:n.-24-18576T=
XR_928319.1:n.750-18576T=
XR_928319.2:n.365-18576T=