Canonical Allele Identifier: CA2396046885

Gene: GNB1L

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19797500_19797505delinsATCATT , CM000684.2:g.19797500_19797505delinsATCATT	GRCh38
NC_000022.10:g.19785023_19785028delinsATCATT , CM000684.1:g.19785023_19785028delinsATCATT	GRCh37
NC_000022.9:g.18165023_18165028delinsATCATT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000329517.11:c.732+4496_732+4501delinsAATGAT MANE Select	ENSP00000331313.6:n.732+4496_732+4501deli...
ENST00000329517.10:c.732+4496_732+4501delinsAATGAT	ENSP00000331313.6:n.732+4496_732+4501deli...
ENST00000403325.5:c.732+4496_732+4501delinsAATGAT	ENSP00000385154.1:n.732+4496_732+4501deli...
ENST00000405009.5:c.630+4598_630+4603delinsAATGAT	ENSP00000384626.1:n.630+4598_630+4603deli...
ENST00000460402.5:n.700+4496_700+4501delinsAATGAT
NM_053004.2:c.732+4496_732+4501delinsAATGAT	NP_443730.1:n.732+4496_732+4501delinsAATG...
NM_053004.3:c.732+4496_732+4501delinsAATGAT MANE Select	NP_443730.1:n.732+4496_732+4501delinsAATG...