Canonical Allele Identifier: CA15547770
Gene: ANGPT1 HGNC NCBI

Linked Data

dbSNP Id: rs2507800

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.107250441T>A , CM000670.2:g.107250441T>A GRCh38
NC_000008.10:g.108262669T>A , CM000670.1:g.108262669T>A GRCh37
NC_000008.9:g.108331845T>A NCBI36
NG_029405.1:g.252586A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000517746.6:c.*1414A>T MANE Select ENSP00000428340.1:n.*1414A>T
ENST00000297450.7:c.*1414A>T ENSP00000297450.3:n.*1414A>T
ENST00000517746.5:c.*1414A>T ENSP00000428340.1:n.*1414A>T
NM_001146.3:c.*1414A>T NP_001137.2:n.*1414A>T
NM_001146.4:c.*1414A>T NP_001137.2:n.*1414A>T
NM_001199859.1:c.*1414A>T NP_001186788.1:n.*1414A>T
NM_001199859.2:c.*1414A>T NP_001186788.1:n.*1414A>T
NM_001314051.1:c.*1414A>T NP_001300980.1:n.*1414A>T
XR_928319.1:n.3196A>T
XR_928319.2:n.2811A>T
NM_001146.5:c.*1414A>T MANE Select NP_001137.2:n.*1414A>T
NM_001199859.3:c.*1414A>T NP_001186788.1:n.*1414A>T
NM_001314051.2:c.*1414A>T NP_001300980.1:n.*1414A>T