Canonical Allele Identifier: CA2404041397

Gene: PVALB

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36803497_36803498delinsTG , CM000684.2:g.36803497_36803498delinsTG	GRCh38
NC_000022.10:g.37199541_37199542delinsTG , CM000684.1:g.37199541_37199542delinsTG	GRCh37
NC_000022.9:g.35529487_35529488delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417718.7:c.305-2580_305-2579delinsCA MANE Select	ENSP00000400247.2:n.305-2580_305-2579delinsCA
ENST00000216200.9:c.305-2580_305-2579delinsCA	ENSP00000216200.5:n.305-2580_305-2579delinsCA
ENST00000404171.1:c.209-2580_209-2579delinsCA	ENSP00000386089.1:n.209-2580_209-2579delinsCA
ENST00000406910.6:c.351-2580_351-2579delinsCA
ENST00000417718.6:c.305-2580_305-2579delinsCA	ENSP00000400247.2:n.305-2580_305-2579delinsCA
NM_001315532.1:c.305-2580_305-2579delinsCA	NP_001302461.1:n.305-2580_305-2579delinsCA
NM_002854.2:c.305-2580_305-2579delinsCA	NP_002845.1:n.305-2580_305-2579delinsCA
NM_001315532.2:c.305-2580_305-2579delinsCA MANE Select	NP_001302461.1:n.305-2580_305-2579delinsCA
NM_002854.3:c.305-2580_305-2579delinsCA	NP_002845.1:n.305-2580_305-2579delinsCA