Canonical Allele Identifier: CA221639248
Gene: CKAP5 HGNC NCBI

Linked Data

dbSNP Id: rs975263440
MyVariant Identifiers: chr11:g.46849460C>T (hg19) chr11:g.46827909C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46827909C>T , CM000673.2:g.46827909C>T GRCh38
NC_000011.9:g.46849460C>T , CM000673.1:g.46849460C>T GRCh37
NC_000011.8:g.46806036C>T NCBI36
NG_029924.1:g.23400G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000529230.6:c.-37-6641G>A MANE Select ENSP00000432768.1:n.-37-6641G>A
ENST00000312055.9:c.-37-6641G>A ENSP00000310227.5:n.-37-6641G>A
ENST00000525248.1:n.78-6661G>A
ENST00000529230.5:c.-37-6641G>A ENSP00000432768.1:n.-37-6641G>A
NM_001008938.3:c.-37-6641G>A NP_001008938.1:n.-37-6641G>A
NM_014756.3:c.-37-6641G>A NP_055571.2:n.-37-6641G>A
NM_001008938.4:c.-37-6641G>A MANE Select NP_001008938.1:n.-37-6641G>A
NM_014756.4:c.-37-6641G>A NP_055571.2:n.-37-6641G>A
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