Canonical Allele Identifier: CA127156123
Gene: ACSL6 HGNC NCBI

Linked Data

dbSNP Id: rs11743803

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.131976545A>G , CM000667.2:g.131976545A>G GRCh38
NC_000005.9:g.131312238A>G , CM000667.1:g.131312238A>G GRCh37
NC_000005.8:g.131340137A>G NCBI36
NG_028290.1:g.40524T>C
NG_028290.2:g.40524T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296869.9:c.954+103T>C ENSP00000296869.5:p.=
ENST00000434099.6:c.885+103T>C ENSP00000397507.2:p.=
ENST00000650697.1:c.984+103T>C ENSP00000498444.1:p.=
ENST00000650912.1:c.810+103T>C ENSP00000499071.1:p.=
ENST00000651086.1:c.*1720+103T>C ENSP00000498727.1:p.=
ENST00000651127.1:n.551T>C
ENST00000651250.1:c.885+103T>C ENSP00000498588.1:p.=
ENST00000651269.1:c.*1045+103T>C ENSP00000498492.1:p.=
ENST00000651356.1:c.990+103T>C ENSP00000498260.1:p.=
ENST00000651427.1:c.810+103T>C ENSP00000498263.1:p.=
ENST00000651454.1:n.373+103T>C
ENST00000651597.1:n.915T>C
ENST00000651883.2:c.990+103T>C MANE Select ENSP00000499063.2:p.=
ENST00000652375.1:n.1568+103T>C
ENST00000652424.1:c.990+103T>C ENSP00000498305.1:p.=
ENST00000652469.1:c.990+103T>C ENSP00000498837.1:p.=
ENST00000652493.1:c.990+103T>C ENSP00000498458.1:p.=
ENST00000296869.8:c.990+103T>C ENSP00000296869.4:p.=
ENST00000357096.5:c.810+103T>C ENSP00000349608.1:p.=
ENST00000379240.5:c.915+103T>C ENSP00000368542.1:p.=
ENST00000379244.5:c.915+103T>C ENSP00000368546.1:p.=
ENST00000379246.5:c.948+103T>C ENSP00000368548.1:p.=
ENST00000379255.5:c.810+103T>C ENSP00000368557.1:p.=
ENST00000379264.6:c.990+103T>C ENSP00000368566.2:p.=
ENST00000413683.5:c.915+103T>C ENSP00000415140.1:p.=
ENST00000431707.5:c.855+103T>C ENSP00000413329.1:p.=
ENST00000434099.5:c.810+103T>C ENSP00000397507.1:p.=
ENST00000543479.5:n.960+103T>C ENSP00000442124.2:p.=
NM_001009185.2:c.990+103T>C NP_001009185.1:p.=
NM_001205247.1:c.885+103T>C NP_001192176.1:p.=
NM_001205248.1:c.915+103T>C NP_001192177.1:p.=
NM_001205250.1:c.948+103T>C NP_001192179.1:p.=
NM_001205251.1:c.810+103T>C NP_001192180.1:p.=
NM_015256.3:c.990+103T>C NP_056071.2:p.=
NM_015256.4:c.990+103T>C NP_056071.2:p.=
NM_001009185.3:c.990+103T>C MANE Select NP_001009185.1:p.=
NM_001205247.2:c.885+103T>C NP_001192176.1:p.=
NM_001205248.2:c.915+103T>C NP_001192177.1:p.=
NM_001205251.2:c.810+103T>C NP_001192180.1:p.=