Canonical Allele Identifier: CA2396046857
Gene: GNB1L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19797461_19797464delinsCAAG , CM000684.2:g.19797461_19797464delinsCAAG GRCh38
NC_000022.10:g.19784984_19784987delinsCAAG , CM000684.1:g.19784984_19784987delinsCAAG GRCh37
NC_000022.9:g.18164984_18164987delinsCAAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000329517.11:c.732+4537_732+4540delinsCTTG MANE Select ENSP00000331313.6:n.732+4537_732+4540deli...
ENST00000329517.10:c.732+4537_732+4540delinsCTTG ENSP00000331313.6:n.732+4537_732+4540deli...
ENST00000403325.5:c.732+4537_732+4540delinsCTTG ENSP00000385154.1:n.732+4537_732+4540deli...
ENST00000405009.5:c.630+4639_630+4642delinsCTTG ENSP00000384626.1:n.630+4639_630+4642deli...
ENST00000460402.5:n.700+4537_700+4540delinsCTTG
NM_053004.2:c.732+4537_732+4540delinsCTTG NP_443730.1:n.732+4537_732+4540delinsCTTG...
NM_053004.3:c.732+4537_732+4540delinsCTTG MANE Select NP_443730.1:n.732+4537_732+4540delinsCTTG...
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