Canonical Allele Identifier: CA1939014511
Gene: SHTN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117067959T= , CM000672.2:g.117067959T= GRCh38
NC_000010.10:g.118827470T= , CM000672.1:g.118827470T= GRCh37
NC_000010.9:g.118817460T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392901.10:c.-188-19449A= ENSP00000376635.4:n.-188-19449A=
ENST00000392901.8:c.-188-19449A= ENSP00000376635.4:n.-188-19449A=
NM_001258300.1:c.-188-19449A= NP_001245229.1:n.-188-19449A=