Canonical Allele Identifier: CA1025503348

Gene: PVALB

Linked Data

• gnomAD v3: 22-36803661-ATGGGTGGGTGGG-A
• gnomAD v4: 22-36803661-ATGGGTGGGTGGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36803665_36803676del , CM000684.2:g.36803665_36803676del	GRCh38
NC_000022.10:g.37199709_37199720del , CM000684.1:g.37199709_37199720del	GRCh37
NC_000022.9:g.35529655_35529666del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000417718.7:c.305-2755_305-2744del MANE Select	ENSP00000400247.2:n.305-2755_305-2744del
ENST00000216200.9:c.305-2755_305-2744del	ENSP00000216200.5:n.305-2755_305-2744del
ENST00000404171.1:c.209-2755_209-2744del	ENSP00000386089.1:n.209-2755_209-2744del
ENST00000406910.6:c.351-2755_351-2744del
ENST00000417718.6:c.305-2755_305-2744del	ENSP00000400247.2:n.305-2755_305-2744del
NM_001315532.1:c.305-2755_305-2744del	NP_001302461.1:n.305-2755_305-2744del
NM_002854.2:c.305-2755_305-2744del	NP_002845.1:n.305-2755_305-2744del
NM_001315532.2:c.305-2755_305-2744del MANE Select	NP_001302461.1:n.305-2755_305-2744del
NM_002854.3:c.305-2755_305-2744del	NP_002845.1:n.305-2755_305-2744del