Canonical Allele Identifier: CA1969112310

Gene: CKAP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46827887_46827890delinsTAGG , CM000673.2:g.46827887_46827890delinsTAGG	GRCh38
NC_000011.9:g.46849438_46849441delinsTAGG , CM000673.1:g.46849438_46849441delinsTAGG	GRCh37
NC_000011.8:g.46806014_46806017delinsTAGG	NCBI36
NG_029924.1:g.23419_23422delinsCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529230.6:c.-37-6622_-37-6619delinsCCTA MANE Select	ENSP00000432768.1:n.-37-6622_-37-6619delinsCCTA
ENST00000312055.9:c.-37-6622_-37-6619delinsCCTA	ENSP00000310227.5:n.-37-6622_-37-6619delinsCCTA
ENST00000525248.1:n.78-6642_78-6639delinsCCTA
ENST00000529230.5:c.-37-6622_-37-6619delinsCCTA	ENSP00000432768.1:n.-37-6622_-37-6619delinsCCTA
NM_001008938.3:c.-37-6622_-37-6619delinsCCTA	NP_001008938.1:n.-37-6622_-37-6619delinsCCTA
NM_014756.3:c.-37-6622_-37-6619delinsCCTA	NP_055571.2:n.-37-6622_-37-6619delinsCCTA
NM_001008938.4:c.-37-6622_-37-6619delinsCCTA MANE Select	NP_001008938.1:n.-37-6622_-37-6619delinsCCTA
NM_014756.4:c.-37-6622_-37-6619delinsCCTA	NP_055571.2:n.-37-6622_-37-6619delinsCCTA