Canonical Allele Identifier: CA2147250639
Gene: DLST HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74899026A= , CM000676.2:g.74899026A= GRCh38
NC_000014.8:g.75365729A= , CM000676.1:g.75365729A= GRCh37
NC_000014.7:g.74435482A= NCBI36
NG_030313.1:g.22136A=

Transcript Alleles

HGVS Amino-acid Change
NM_001933.5:c.901+527A= MANE Select NP_001924.2:n.901+527A=
ENST00000334220.9:c.901+527A= MANE Select ENSP00000335304.4:n.901+527A=
NM_001933.4:c.901+527A= NP_001924.2:n.901+527A=
NR_033814.1:n.906+527A=
NR_033814.2:n.881+527A=
NR_045209.1:n.915+527A=
NR_045209.2:n.890+527A=
ENST00000238671.11:c.*639+527A= ENSP00000238671.7:n.*639+527A=
ENST00000334220.8:c.901+527A= ENSP00000335304.4:n.901+527A=
ENST00000554612.5:c.*644+527A= ENSP00000451670.1:n.*644+527A=
ENST00000555089.5:c.*530+527A= ENSP00000452422.1:n.*530+527A=
XR_001750184.2:n.844+527A=