Canonical Allele Identifier: CA1969112099

Gene: CKAP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46827365A= , CM000673.2:g.46827365A=	GRCh38
NC_000011.9:g.46848916A= , CM000673.1:g.46848916A=	GRCh37
NC_000011.8:g.46805492A=	NCBI36
NG_029924.1:g.23944T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529230.6:c.-37-6097T= MANE Select	ENSP00000432768.1:n.-37-6097T=
ENST00000312055.9:c.-37-6097T=	ENSP00000310227.5:n.-37-6097T=
ENST00000525248.1:n.78-6117T=
ENST00000529230.5:c.-37-6097T=	ENSP00000432768.1:n.-37-6097T=
NM_001008938.3:c.-37-6097T=	NP_001008938.1:n.-37-6097T=
NM_014756.3:c.-37-6097T=	NP_055571.2:n.-37-6097T=
NM_001008938.4:c.-37-6097T= MANE Select	NP_001008938.1:n.-37-6097T=
NM_014756.4:c.-37-6097T=	NP_055571.2:n.-37-6097T=