Canonical Allele Identifier: CA1210236700

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354494_179354496delinsTTG , CM000663.2:g.179354494_179354496delinsTTG	GRCh38
NC_000001.10:g.179323629_179323631delinsTTG , CM000663.1:g.179323629_179323631delinsTTG	GRCh37
NC_000001.9:g.177590252_177590254delinsTTG	NCBI36
NG_030638.1:g.65781_65783delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*853_*855delinsTTG MANE Select	ENSP00000356591.3:n.*853_*855delinsTTG
ENST00000367619.7:c.*853_*855delinsTTG	ENSP00000356591.3:n.*853_*855delinsTTG
ENST00000539888.5:c.*853_*855delinsTTG	ENSP00000441356.1:n.*853_*855delinsTTG
ENST00000540564.5:c.*853_*855delinsTTG	ENSP00000445315.1:n.*853_*855delinsTTG
NM_001252511.1:c.*853_*855delinsTTG	NP_001239440.1:n.*853_*855delinsTTG
NM_001252512.1:c.*853_*855delinsTTG	NP_001239441.1:n.*853_*855delinsTTG
NM_003101.5:c.*853_*855delinsTTG	NP_003092.4:n.*853_*855delinsTTG
NR_045530.1:n.2656_2658delinsTTG
XM_011509911.1:c.*853_*855delinsTTG	XP_011508213.1:n.*853_*855delinsTTG
NM_003101.6:c.*853_*855delinsTTG MANE Select	NP_003092.4:n.*853_*855delinsTTG
NR_045530.2:n.2573_2575delinsTTG
NM_001252511.2:c.*853_*855delinsTTG	NP_001239440.1:n.*853_*855delinsTTG
NM_001252512.2:c.*853_*855delinsTTG	NP_001239441.1:n.*853_*855delinsTTG