Canonical Allele Identifier: CA1025503474

Gene: PVALB

Linked Data

• gnomAD v3: 22-36803696-GAT-G
• gnomAD v4: 22-36803696-GAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36803697_36803698del , CM000684.2:g.36803697_36803698del	GRCh38
NC_000022.10:g.37199741_37199742del , CM000684.1:g.37199741_37199742del	GRCh37
NC_000022.9:g.35529687_35529688del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417718.7:c.305-2780_305-2779del MANE Select	ENSP00000400247.2:n.305-2780_305-2779del
ENST00000216200.9:c.305-2780_305-2779del	ENSP00000216200.5:n.305-2780_305-2779del
ENST00000404171.1:c.209-2780_209-2779del	ENSP00000386089.1:n.209-2780_209-2779del
ENST00000406910.6:c.351-2780_351-2779del
ENST00000417718.6:c.305-2780_305-2779del	ENSP00000400247.2:n.305-2780_305-2779del
NM_001315532.1:c.305-2780_305-2779del	NP_001302461.1:n.305-2780_305-2779del
NM_002854.2:c.305-2780_305-2779del	NP_002845.1:n.305-2780_305-2779del
NM_001315532.2:c.305-2780_305-2779del MANE Select	NP_001302461.1:n.305-2780_305-2779del
NM_002854.3:c.305-2780_305-2779del	NP_002845.1:n.305-2780_305-2779del