Canonical Allele Identifier: CA788486263
Gene:

Linked Data

dbSNP Id: rs1434935430
MyVariant Identifiers: chr4:g.145480443_145480444insTAG (hg19) chr4:g.144559291_144559292insTAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559291_144559292insTAG , CM000666.2:g.144559291_144559292insTAG GRCh38
NC_000004.11:g.145480443_145480444insTAG , CM000666.1:g.145480443_145480444insTAG GRCh37
NC_000004.10:g.145699893_145699894insTAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143314_328-143313insCTA ENSP00000497507.1:n.328-143314_328-143313insCTA
XR_939272.1:n.178+2692_178+2693insCTA
XR_939273.1:n.178+2692_178+2693insCTA
XR_939272.2:n.522+2692_522+2693insCTA
XR_939273.2:n.522+2692_522+2693insCTA
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