Canonical Allele Identifier: CA221639124

Gene: CKAP5

Linked Data

• dbSNP Id: rs762411348
• MyVariant Identifiers: chr11:g.46849298A>C (hg19) ; chr11:g.46827747A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46827747A>C , CM000673.2:g.46827747A>C	GRCh38
NC_000011.9:g.46849298A>C , CM000673.1:g.46849298A>C	GRCh37
NC_000011.8:g.46805874A>C	NCBI36
NG_029924.1:g.23562T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529230.6:c.-37-6479T>G MANE Select	ENSP00000432768.1:n.-37-6479T>G
ENST00000312055.9:c.-37-6479T>G	ENSP00000310227.5:n.-37-6479T>G
ENST00000525248.1:n.78-6499T>G
ENST00000529230.5:c.-37-6479T>G	ENSP00000432768.1:n.-37-6479T>G
NM_001008938.3:c.-37-6479T>G	NP_001008938.1:n.-37-6479T>G
NM_014756.3:c.-37-6479T>G	NP_055571.2:n.-37-6479T>G
NM_001008938.4:c.-37-6479T>G MANE Select	NP_001008938.1:n.-37-6479T>G
NM_014756.4:c.-37-6479T>G	NP_055571.2:n.-37-6479T>G