Canonical Allele Identifier: CA2657554454

Gene: NCAPH2

Linked Data

• gnomAD v4: 22-50523550-A-ATC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50523551_50523552dup , CM000684.2:g.50523551_50523552dup	GRCh38
NC_000022.10:g.50961980_50961981dup , CM000684.1:g.50961980_50961981dup	GRCh37
NC_000022.9:g.49308846_49308847dup	NCBI36
NG_016235.1:g.7888_7889dup
NG_021419.1:g.20336_20337dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420993.7:c.*176_*177dup MANE Select	ENSP00000410088.2:n.*176_*177dup
NM_001185011.1:c.*176_*177dup	NP_001171940.1:n.*176_*177dup
NM_152299.3:c.*176_*177dup	NP_689512.2:n.*176_*177dup
XR_001755232.1:n.2204_2205dup
NM_152299.4:c.*176_*177dup MANE Select	NP_689512.2:n.*176_*177dup
NM_001185011.2:c.*176_*177dup	NP_001171940.1:n.*176_*177dup