Canonical Allele Identifier: CA707371221
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs1274932721
MyVariant Identifiers: chr14:g.61112224_61112225insT (hg19) chr14:g.60645506_60645507insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60645509dup , CM000676.2:g.60645509dup GRCh38
NC_000014.8:g.61112227dup , CM000676.1:g.61112227dup GRCh37
NC_000014.7:g.60181980dup NCBI36
NG_008231.1:g.8931dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.*776dup MANE Select ENSP00000494686.1:n.*776dup
ENST00000247182.6:c.*776dup ENSP00000247182.5:n.*776dup
ENST00000553535.2:n.1319dup
ENST00000554986.2:c.*776dup ENSP00000452700.2:n.*776dup
ENST00000555955.3:n.2268dup
NM_005982.3:c.*776dup NP_005973.1:n.*776dup
XM_017021602.2:c.*1050dup XP_016877091.1:n.*1050dup
NM_005982.4:c.*776dup MANE Select NP_005973.1:n.*776dup
Search 100 bp 5'
Search 100 bp 3'