Canonical Allele Identifier: CA752872666
Gene: PVALB HGNC NCBI

Linked Data

dbSNP Id: rs1555910551

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36803673_36803674insGGGA , CM000684.2:g.36803673_36803674insGGGA GRCh38
NC_000022.10:g.37199717_37199718insGGGA , CM000684.1:g.37199717_37199718insGGGA GRCh37
NC_000022.9:g.35529663_35529664insGGGA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000417718.7:c.305-2756_305-2755insTCCC MANE Select ENSP00000400247.2:n.305-2756_305-2755insT...
ENST00000216200.9:c.305-2756_305-2755insTCCC ENSP00000216200.5:n.305-2756_305-2755insT...
ENST00000404171.1:c.209-2756_209-2755insTCCC ENSP00000386089.1:n.209-2756_209-2755insT...
ENST00000406910.6:c.351-2756_351-2755insTCCC
ENST00000417718.6:c.305-2756_305-2755insTCCC ENSP00000400247.2:n.305-2756_305-2755insT...
NM_001315532.1:c.305-2756_305-2755insTCCC NP_001302461.1:n.305-2756_305-2755insTCCC...
NM_002854.2:c.305-2756_305-2755insTCCC NP_002845.1:n.305-2756_305-2755insTCCC
NM_001315532.2:c.305-2756_305-2755insTCCC MANE Select NP_001302461.1:n.305-2756_305-2755insTCCC...
NM_002854.3:c.305-2756_305-2755insTCCC NP_002845.1:n.305-2756_305-2755insTCCC