Canonical Allele Identifier: CA676946696

Gene: CKAP5

Linked Data

• dbSNP Id: rs1353156362
• MyVariant Identifiers: chr11:g.46848918T>G (hg19) ; chr11:g.46827367T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46827367T>G , CM000673.2:g.46827367T>G	GRCh38
NC_000011.9:g.46848918T>G , CM000673.1:g.46848918T>G	GRCh37
NC_000011.8:g.46805494T>G	NCBI36
NG_029924.1:g.23942A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529230.6:c.-37-6099A>C MANE Select	ENSP00000432768.1:n.-37-6099A>C
ENST00000312055.9:c.-37-6099A>C	ENSP00000310227.5:n.-37-6099A>C
ENST00000525248.1:n.78-6119A>C
ENST00000529230.5:c.-37-6099A>C	ENSP00000432768.1:n.-37-6099A>C
NM_001008938.3:c.-37-6099A>C	NP_001008938.1:n.-37-6099A>C
NM_014756.3:c.-37-6099A>C	NP_055571.2:n.-37-6099A>C
NM_001008938.4:c.-37-6099A>C MANE Select	NP_001008938.1:n.-37-6099A>C
NM_014756.4:c.-37-6099A>C	NP_055571.2:n.-37-6099A>C