Canonical Allele Identifier: CA261719965
Gene: SIX1 HGNC NCBI

Linked Data

dbSNP Id: rs751939659
MyVariant Identifiers: chr14:g.61112290_61112291insA (hg19) chr14:g.60645572_60645573insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60645577dup , CM000676.2:g.60645577dup GRCh38
NC_000014.8:g.61112295dup , CM000676.1:g.61112295dup GRCh37
NC_000014.7:g.60182048dup NCBI36
NG_008231.1:g.8865dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000645694.3:c.*710dup MANE Select ENSP00000494686.1:n.*710dup
ENST00000247182.6:c.*710dup ENSP00000247182.5:n.*710dup
ENST00000553535.2:n.1253dup
ENST00000554986.2:c.*710dup ENSP00000452700.2:n.*710dup
ENST00000555955.3:n.2202dup
NM_005982.3:c.*710dup NP_005973.1:n.*710dup
XM_017021602.2:c.*984dup XP_016877091.1:n.*984dup
NM_005982.4:c.*710dup MANE Select NP_005973.1:n.*710dup
Search 100 bp 5'
Search 100 bp 3'