Canonical Allele Identifier: CA2410905765

Gene: NCAPH2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50523563_50523566delinsACAG , CM000684.2:g.50523563_50523566delinsACAG	GRCh38
NC_000022.10:g.50961992_50961995delinsACAG , CM000684.1:g.50961992_50961995delinsACAG	GRCh37
NC_000022.9:g.49308858_49308861delinsACAG	NCBI36
NG_016235.1:g.7874_7877delinsCTGT
NG_021419.1:g.20348_20351delinsACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420993.7:c.*188_*191delinsACAG MANE Select	ENSP00000410088.2:n.*188_*191delinsACAG
NM_001185011.1:c.*188_*191delinsACAG	NP_001171940.1:n.*188_*191delinsACAG
NM_152299.3:c.*188_*191delinsACAG	NP_689512.2:n.*188_*191delinsACAG
XR_001755232.1:n.2216_2219delinsACAG
NM_152299.4:c.*188_*191delinsACAG MANE Select	NP_689512.2:n.*188_*191delinsACAG
NM_001185011.2:c.*188_*191delinsACAG	NP_001171940.1:n.*188_*191delinsACAG