Canonical Allele Identifier: CA2172180627

Gene: CHP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41271770_41271771delinsAT , CM000677.2:g.41271770_41271771delinsAT	GRCh38
NC_000015.9:g.41563968_41563969delinsAT , CM000677.1:g.41563968_41563969delinsAT	GRCh37
NC_000015.8:g.39351260_39351261delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334660.10:c.411+1152_411+1153delinsAT MANE Select	ENSP00000335632.5:n.411+1152_411+1153delinsAT
ENST00000334660.9:c.411+1152_411+1153delinsAT	ENSP00000335632.5:n.411+1152_411+1153delinsAT
ENST00000392151.6:c.350-6997_350-6996delinsAT	ENSP00000440490.1:n.350-6997_350-6996delinsAT
ENST00000558351.5:n.543+1152_543+1153delinsAT
ENST00000560397.5:c.411+1152_411+1153delinsAT	ENSP00000454007.1:n.411+1152_411+1153delinsAT
ENST00000560411.5:c.*176+1152_*176+1153delinsAT	ENSP00000453375.1:n.*176+1152_*176+1153delinsAT
ENST00000560633.1:n.399-410_399-409delinsAT
ENST00000560784.5:c.*110+1152_*110+1153delinsAT	ENSP00000452772.1:n.*110+1152_*110+1153delinsAT
ENST00000560965.1:c.272-410_272-409delinsAT
NM_007236.4:c.411+1152_411+1153delinsAT	NP_009167.1:n.411+1152_411+1153delinsAT
NM_007236.5:c.411+1152_411+1153delinsAT MANE Select	NP_009167.1:n.411+1152_411+1153delinsAT