Canonical Allele Identifier: CA14940175

Gene: PVALB

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36812105G>T , CM000684.2:g.36812105G>T	GRCh38
NC_000022.10:g.37208149G>T , CM000684.1:g.37208149G>T	GRCh37
NC_000022.9:g.35538095G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417718.7:c.304+1541C>A MANE Select	ENSP00000400247.2:n.304+1541C>A
ENST00000216200.9:c.304+1541C>A	ENSP00000216200.5:n.304+1541C>A
ENST00000404171.1:c.208+1541C>A	ENSP00000386089.1:n.208+1541C>A
ENST00000406910.6:c.301-581C>A
ENST00000417718.6:c.304+1541C>A	ENSP00000400247.2:n.304+1541C>A
NM_001315532.1:c.304+1541C>A	NP_001302461.1:n.304+1541C>A
NM_002854.2:c.304+1541C>A	NP_002845.1:n.304+1541C>A
XM_011530288.1:c.305-581C>A	XP_011528590.1:n.305-581C>A
NM_001315532.2:c.304+1541C>A MANE Select	NP_001302461.1:n.304+1541C>A
NM_002854.3:c.304+1541C>A	NP_002845.1:n.304+1541C>A